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FDA 510(k)

MAXI COMPRESSORS

K-Number: K900686 · 1990-04-26

ApplicantMedical Industries America, Inc.
Decision Date1990-04-26
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MAXI COMPRESSORS 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 1990-04-26 under 510(k) number K900686. 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 MAXI COMPRESSORS?

MAXI COMPRESSORS is a medical device that received FDA 510(k) clearance on 1990-04-26. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K900686.

When did MAXI COMPRESSORS receive FDA 510(k) clearance?

MAXI COMPRESSORS received FDA 510(k) clearance on 1990-04-26, under 510(k) number K900686.

Who is the listed applicant for MAXI COMPRESSORS?

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 MAXI COMPRESSORS?

The FDA product code for MAXI COMPRESSORS 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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