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FDA 510(k)

A-GENT GLYCOSPEC

K-Number: K791642 · 1979-10-17

ApplicantAbbott Laboratories
Decision Date1979-10-17
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

A-GENT GLYCOSPEC is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-10-17 under 510(k) number K791642. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-GENT GLYCOSPEC?

A-GENT GLYCOSPEC is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Abbott Laboratories. The 510(k) number is K791642.

When did A-GENT GLYCOSPEC receive FDA 510(k) clearance?

A-GENT GLYCOSPEC received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791642.

Who is the listed applicant for A-GENT GLYCOSPEC?

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

What is the FDA product code for A-GENT GLYCOSPEC?

The FDA product code for A-GENT GLYCOSPEC is LCP.

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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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