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FDA 510(k)

ANTIBODY TO HERPESVIRUS HOMINIS

K-Number: K791058 · 1979-09-07

ApplicantElectro-Nucleonics Laboratories, Inc.
Decision Date1979-09-07
Product CodeGQO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIBODY TO HERPESVIRUS HOMINIS is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Nucleonics Laboratories, Inc.. It received FDA 510(k) clearance on 1979-09-07 under 510(k) number K791058. 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 ANTIBODY TO HERPESVIRUS HOMINIS?

ANTIBODY TO HERPESVIRUS HOMINIS is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Electro-Nucleonics Laboratories, Inc.. The 510(k) number is K791058.

When did ANTIBODY TO HERPESVIRUS HOMINIS receive FDA 510(k) clearance?

ANTIBODY TO HERPESVIRUS HOMINIS received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791058.

Who is the listed applicant for ANTIBODY TO HERPESVIRUS HOMINIS?

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

What is the FDA product code for ANTIBODY TO HERPESVIRUS HOMINIS?

The FDA product code for ANTIBODY TO HERPESVIRUS HOMINIS is GQO.

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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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