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FDA 510(k)

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL

K-Number: K822711 · 1982-11-03

ApplicantParker Laboratories, Inc.
Decision Date1982-11-03
Product CodeFAX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K822711. The device is classified under product code FAX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL?

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K822711.

When did ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL receive FDA 510(k) clearance?

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822711.

Who is the listed applicant for ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL?

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

What is the FDA product code for ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL?

The FDA product code for ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL is FAX.

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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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