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FDA 510(k)

GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I

K-Number: K810043 · 1981-05-15

ApplicantVibac Corp.
Decision Date1981-05-15
Product CodeGQM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I is the device name listed in this FDA 510(k) record. The listed applicant is Vibac Corp.. It received FDA 510(k) clearance on 1981-05-15 under 510(k) number K810043. The device is classified under product code GQM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I?

GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I is a medical device that received FDA 510(k) clearance on 1981-05-15. The listed applicant is Vibac Corp.. The 510(k) number is K810043.

When did GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I receive FDA 510(k) clearance?

GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I received FDA 510(k) clearance on 1981-05-15, under 510(k) number K810043.

Who is the listed applicant for GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I?

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

What is the FDA product code for GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I?

The FDA product code for GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I is GQM.

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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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