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FDA 510(k)

MODEL IRC 1001 AEROSOL COMPRESSOR

K-Number: K992643 · 1999-10-27

ApplicantInvacare Corp.
Decision Date1999-10-27
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL IRC 1001 AEROSOL COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1999-10-27 under 510(k) number K992643. 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 MODEL IRC 1001 AEROSOL COMPRESSOR?

MODEL IRC 1001 AEROSOL COMPRESSOR is a medical device that received FDA 510(k) clearance on 1999-10-27. The listed applicant is Invacare Corp.. The 510(k) number is K992643.

When did MODEL IRC 1001 AEROSOL COMPRESSOR receive FDA 510(k) clearance?

MODEL IRC 1001 AEROSOL COMPRESSOR received FDA 510(k) clearance on 1999-10-27, under 510(k) number K992643.

Who is the listed applicant for MODEL IRC 1001 AEROSOL COMPRESSOR?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL IRC 1001 AEROSOL COMPRESSOR?

The FDA product code for MODEL IRC 1001 AEROSOL COMPRESSOR is 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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