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FDA 510(k)

COMPRESSOR

K-Number: K792457 · 1980-02-05

ApplicantPneupac , Ltd.
Decision Date1980-02-05
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPRESSOR 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 K792457. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSOR?

COMPRESSOR 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 K792457.

When did COMPRESSOR receive FDA 510(k) clearance?

COMPRESSOR received FDA 510(k) clearance on 1980-02-05, under 510(k) number K792457.

Who is the listed applicant for COMPRESSOR?

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 COMPRESSOR?

The FDA product code for COMPRESSOR is BTI.

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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: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, Inc.

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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