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FDA 510(k)

AM-50 AEROSOL/MEDICATION AIR COMPRESSOR

K-Number: K945478 · 1995-09-28

ApplicantPreferred Medical Supply, Inc.
Decision Date1995-09-28
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AM-50 AEROSOL/MEDICATION AIR COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Medical Supply, Inc.. It received FDA 510(k) clearance on 1995-09-28 under 510(k) number K945478. 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 AM-50 AEROSOL/MEDICATION AIR COMPRESSOR?

AM-50 AEROSOL/MEDICATION AIR COMPRESSOR is a medical device that received FDA 510(k) clearance on 1995-09-28. The listed applicant is Preferred Medical Supply, Inc.. The 510(k) number is K945478.

When did AM-50 AEROSOL/MEDICATION AIR COMPRESSOR receive FDA 510(k) clearance?

AM-50 AEROSOL/MEDICATION AIR COMPRESSOR received FDA 510(k) clearance on 1995-09-28, under 510(k) number K945478.

Who is the listed applicant for AM-50 AEROSOL/MEDICATION AIR COMPRESSOR?

The FDA 510(k) record lists Preferred Medical Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AM-50 AEROSOL/MEDICATION AIR COMPRESSOR?

The FDA product code for AM-50 AEROSOL/MEDICATION AIR COMPRESSOR is BTI.

Related Clinical Trials

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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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