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FDA 510(k)

INSTANT AIR

K-Number: K771587 · 1977-09-02

ApplicantHyde, Vernon E., D.D.S.
Decision Date1977-09-02
Product CodeBWC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSTANT AIR is the device name listed in this FDA 510(k) record. The listed applicant is Hyde, Vernon E., D.D.S.. It received FDA 510(k) clearance on 1977-09-02 under 510(k) number K771587. The device is classified under product code BWC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTANT AIR?

INSTANT AIR is a medical device that received FDA 510(k) clearance on 1977-09-02. The listed applicant is Hyde, Vernon E., D.D.S.. The 510(k) number is K771587.

When did INSTANT AIR receive FDA 510(k) clearance?

INSTANT AIR received FDA 510(k) clearance on 1977-09-02, under 510(k) number K771587.

Who is the listed applicant for INSTANT AIR?

The FDA 510(k) record lists Hyde, Vernon E., D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTANT AIR?

The FDA product code for INSTANT AIR is BWC.

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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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