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FDA 510(k)

COMPRESSED AIR & OXYGEN GEN./DELIVERY SY

K-Number: K803232 · 1981-02-02

ApplicantDri-Aire, Inc.
Decision Date1981-02-02
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPRESSED AIR & OXYGEN GEN./DELIVERY SY is the device name listed in this FDA 510(k) record. The listed applicant is Dri-Aire, Inc.. It received FDA 510(k) clearance on 1981-02-02 under 510(k) number K803232. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSED AIR & OXYGEN GEN./DELIVERY SY?

COMPRESSED AIR & OXYGEN GEN./DELIVERY SY is a medical device that received FDA 510(k) clearance on 1981-02-02. The listed applicant is Dri-Aire, Inc.. The 510(k) number is K803232.

When did COMPRESSED AIR & OXYGEN GEN./DELIVERY SY receive FDA 510(k) clearance?

COMPRESSED AIR & OXYGEN GEN./DELIVERY SY received FDA 510(k) clearance on 1981-02-02, under 510(k) number K803232.

Who is the listed applicant for COMPRESSED AIR & OXYGEN GEN./DELIVERY SY?

The FDA 510(k) record lists Dri-Aire, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPRESSED AIR & OXYGEN GEN./DELIVERY SY?

The FDA product code for COMPRESSED AIR & OXYGEN GEN./DELIVERY SY is CAW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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