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FDA 510(k)

HERPES I.D. TM TEST

K-Number: K771445 · 1977-12-14

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1977-12-14
Product CodeGQL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HERPES I.D. TM TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1977-12-14 under 510(k) number K771445. The device is classified under product code GQL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERPES I.D. TM TEST?

HERPES I.D. TM TEST is a medical device that received FDA 510(k) clearance on 1977-12-14. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K771445.

When did HERPES I.D. TM TEST receive FDA 510(k) clearance?

HERPES I.D. TM TEST received FDA 510(k) clearance on 1977-12-14, under 510(k) number K771445.

Who is the listed applicant for HERPES I.D. TM TEST?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HERPES I.D. TM TEST?

The FDA product code for HERPES I.D. TM TEST is GQL.

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Related Devices (Code: GQL)

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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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