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FDA 510(k)

ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2

K-Number: K842663 · 1985-12-06

ApplicantAmico Lab, Inc.
Decision Date1985-12-06
Product CodeGQO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 is the device name listed in this FDA 510(k) record. The listed applicant is Amico Lab, Inc.. It received FDA 510(k) clearance on 1985-12-06 under 510(k) number K842663. The device is classified under product code GQO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2?

ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Amico Lab, Inc.. The 510(k) number is K842663.

When did ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 receive FDA 510(k) clearance?

ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 received FDA 510(k) clearance on 1985-12-06, under 510(k) number K842663.

Who is the listed applicant for ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2?

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

What is the FDA product code for ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2?

The FDA product code for ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 is GQO.

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Other records listing Amico Lab, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K842662ANTI-EPSTEIN-BARR VIRUS KITK842530AMIZYME-EBV TEST KITK842661ANTI-CYTOMEGALOVIRUS KITK842531AMIZYME-HSV TYPES 1 & 2 TEST KITSK842529AMIZYME-CMV KITK842660ANTI-SCHISTOSOMA SPECIES KIT

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Related Devices (Code: GQO)

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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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