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FDA 510(k)

GIBCO HERPES ID KIT

K-Number: K841943 · 1985-03-13

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1985-03-13
Product CodeGQL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GIBCO HERPES ID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1985-03-13 under 510(k) number K841943. 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 GIBCO HERPES ID KIT?

GIBCO HERPES ID KIT is a medical device that received FDA 510(k) clearance on 1985-03-13. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K841943.

When did GIBCO HERPES ID KIT receive FDA 510(k) clearance?

GIBCO HERPES ID KIT received FDA 510(k) clearance on 1985-03-13, under 510(k) number K841943.

Who is the listed applicant for GIBCO HERPES ID KIT?

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

What is the FDA product code for GIBCO HERPES ID KIT?

The FDA product code for GIBCO HERPES ID KIT 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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