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FDA 510(k)

HLR QUICK-FIT HEART-LUNG RESUSCITATOR

K-Number: K761194 · 1976-12-09

ApplicantMckesson Corp.
Decision Date1976-12-09
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HLR QUICK-FIT HEART-LUNG RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mckesson Corp.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761194. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HLR QUICK-FIT HEART-LUNG RESUSCITATOR?

HLR QUICK-FIT HEART-LUNG RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Mckesson Corp.. The 510(k) number is K761194.

When did HLR QUICK-FIT HEART-LUNG RESUSCITATOR receive FDA 510(k) clearance?

HLR QUICK-FIT HEART-LUNG RESUSCITATOR received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761194.

Who is the listed applicant for HLR QUICK-FIT HEART-LUNG RESUSCITATOR?

The FDA 510(k) record lists Mckesson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HLR QUICK-FIT HEART-LUNG RESUSCITATOR?

The FDA product code for HLR QUICK-FIT HEART-LUNG RESUSCITATOR is DRM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Mckesson Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K771175RESUSCITATOR, MS30K761196NITROUS OXIDE SCAVENGING MASKK761195ESOPHAGEAL OBTURATION AIRWAYK760017CONSIOUS SEDATION (ANALOR P-76)

Related Devices (Code: DRM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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