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FDA 510(k)

MAXI ASPIRATOR

K-Number: K902184 · 1991-02-12

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

Device Summary

MAXI ASPIRATOR 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 K902184. 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 ASPIRATOR?

MAXI ASPIRATOR 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 K902184.

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

MAXI ASPIRATOR received FDA 510(k) clearance on 1991-02-12, under 510(k) number K902184.

Who is the listed applicant for MAXI ASPIRATOR?

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 ASPIRATOR?

The FDA product code for MAXI ASPIRATOR is BTI.

Related Clinical Trials

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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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