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FDA 510(k)

#504 MINI COMPRESSOR

K-Number: K904045 · 1991-02-12

ApplicantMedical Industries America, Inc.
Decision Date1991-02-12
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

#504 MINI COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Industries America, Inc.. It received FDA 510(k) clearance on 1991-02-12 under 510(k) number K904045. 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 #504 MINI COMPRESSOR?

#504 MINI COMPRESSOR is a medical device that received FDA 510(k) clearance on 1991-02-12. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K904045.

When did #504 MINI COMPRESSOR receive FDA 510(k) clearance?

#504 MINI COMPRESSOR received FDA 510(k) clearance on 1991-02-12, under 510(k) number K904045.

Who is the listed applicant for #504 MINI COMPRESSOR?

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

What is the FDA product code for #504 MINI COMPRESSOR?

The FDA product code for #504 MINI COMPRESSOR is BTI.

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Other records listing Medical Industries America, Inc. 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.

K050990REMREST HEATED HUMIDIFIERK032170TRANSNEB COMPRESSOR W/NEBULIZER, MODEL 5000K002763REMRESTK011053OPTIMAK9640783050 SPORT-NEBK9439903000 AEROSOL TWO

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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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