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FDA 510(k)

3002 AEROMAX

K-Number: K942444 · 1995-03-10

ApplicantMedical Industries America, Inc.
Decision Date1995-03-10
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

3002 AEROMAX 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 1995-03-10 under 510(k) number K942444. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3002 AEROMAX?

3002 AEROMAX is a medical device that received FDA 510(k) clearance on 1995-03-10. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K942444.

When did 3002 AEROMAX receive FDA 510(k) clearance?

3002 AEROMAX received FDA 510(k) clearance on 1995-03-10, under 510(k) number K942444.

Who is the listed applicant for 3002 AEROMAX?

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 3002 AEROMAX?

The FDA product code for 3002 AEROMAX is CAF.

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Other records listing Medical Industries America, Inc. as applicant

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

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Related Devices (Code: CAF)

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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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