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FDA 510(k)

SALTER AIRE COMPRESSOR

K-Number: K992285 · 2000-01-07

ApplicantSalter Labs
Decision Date2000-01-07
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SALTER AIRE COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 2000-01-07 under 510(k) number K992285. 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 SALTER AIRE COMPRESSOR?

SALTER AIRE COMPRESSOR is a medical device that received FDA 510(k) clearance on 2000-01-07. The listed applicant is Salter Labs. The 510(k) number is K992285.

When did SALTER AIRE COMPRESSOR receive FDA 510(k) clearance?

SALTER AIRE COMPRESSOR received FDA 510(k) clearance on 2000-01-07, under 510(k) number K992285.

Who is the listed applicant for SALTER AIRE COMPRESSOR?

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

What is the FDA product code for SALTER AIRE COMPRESSOR?

The FDA product code for SALTER AIRE 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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