![]() 238000006073 displacement reaction Methods 0.000 description 6.208000010125 Myocardial Infarction Diseases 0.000 description 6.238000007906 compression Methods 0.000 claims abstract description 156.238000009423 ventilation Methods 0.000 claims abstract description 210.238000002680 cardiopulmonary resuscitation Methods 0.000 title claims abstract description 58.Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.) Filing date Publication date Application filed by Ludwik Nowakowski filed Critical Ludwik Nowakowski Priority to US08/008,317 priority Critical patent/US5327887A/en Application granted granted Critical Publication of US5327887A publication Critical patent/US5327887A/en Anticipated expiration legal-status Critical Status Expired - Fee Related legal-status Critical Current Links Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Expired - Fee Related Application number US08/008,317 Inventor Ludwik Nowakowski Original Assignee Ludwik Nowakowski Priority date (The priority date is an assumption and is not a legal conclusion. Google Patents Cardiopulmonary resuscitation deviceĭownload PDF Info Publication number US5327887A US5327887A US08/008,317 US831793A US5327887A US 5327887 A US5327887 A US 5327887A US 831793 A US831793 A US 831793A US 5327887 A US5327887 A US 5327887A Authority US United States Prior art keywords patient ventilation chest thumper compression Prior art date Legal status (The legal status is an assumption and is not a legal conclusion. Google Patents US5327887A - Cardiopulmonary resuscitation device Learn more about medical device recalls.Ģ Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.ģ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.ĥ10(K)s with Product Code = DRM and Original Applicant = MICHIGAN INSTRUMENTS, INC.US5327887A - Cardiopulmonary resuscitation device ![]() The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. The Japanese distributor is instructed by letter dated 9/14/06 to drill a small hole in the male checked connector at the base of the column in order to allow rapid bleed off of the pressure and to give customers a revised operators manual.ġ A record in this database is created when a firm initiates a correction or removal action. 7-xxxx or 9-xxxx).įailure to initiate compressions when turned on. Michigan Instruments Thumper Mechanical CPR Device Model 1007, Part number 15000.Īll units sold in Japan (All serial numbers with 7- or 9- followed by 4 numbers e.g.
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