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FDA 510(k)

PNEUPAC RESUSCITATOR INSTANT ACTION SET

K-Number: K792452 · 1980-02-05

ApplicantPneupac , Ltd.
Decision Date1980-02-05
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PNEUPAC RESUSCITATOR INSTANT ACTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Pneupac , Ltd.. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K792452. 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 PNEUPAC RESUSCITATOR INSTANT ACTION SET?

PNEUPAC RESUSCITATOR INSTANT ACTION SET is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Pneupac , Ltd.. The 510(k) number is K792452.

When did PNEUPAC RESUSCITATOR INSTANT ACTION SET receive FDA 510(k) clearance?

PNEUPAC RESUSCITATOR INSTANT ACTION SET received FDA 510(k) clearance on 1980-02-05, under 510(k) number K792452.

Who is the listed applicant for PNEUPAC RESUSCITATOR INSTANT ACTION SET?

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

What is the FDA product code for PNEUPAC RESUSCITATOR INSTANT ACTION SET?

The FDA product code for PNEUPAC RESUSCITATOR INSTANT ACTION SET is DRM.

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Other records listing Pneupac , Ltd. 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.

K040090COMPPAC 200HD; CS12 POWER SUPPLY (AIRCRAFT/VECHILE); PS11 POWER SUPPLY (MAINS)K030803PARAPAC 200D TRANSPORT, MODEL V200DK021841COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGERK020899PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200DK960515PARAPACK863410PATIENT VALVE WITH AIR ENTRAINMENT

View all 19 devices →

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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