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FDA 510(k)

A-GENT(TM) LIQUID GLUCOSE TRINDER

K-Number: K863948 · 1986-11-13

ApplicantAbbott Laboratories
Decision Date1986-11-13
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

A-GENT(TM) LIQUID GLUCOSE TRINDER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1986-11-13 under 510(k) number K863948. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-GENT(TM) LIQUID GLUCOSE TRINDER?

A-GENT(TM) LIQUID GLUCOSE TRINDER is a medical device that received FDA 510(k) clearance on 1986-11-13. The listed applicant is Abbott Laboratories. The 510(k) number is K863948.

When did A-GENT(TM) LIQUID GLUCOSE TRINDER receive FDA 510(k) clearance?

A-GENT(TM) LIQUID GLUCOSE TRINDER received FDA 510(k) clearance on 1986-11-13, under 510(k) number K863948.

Who is the listed applicant for A-GENT(TM) LIQUID GLUCOSE TRINDER?

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(TM) LIQUID GLUCOSE TRINDER?

The FDA product code for A-GENT(TM) LIQUID GLUCOSE TRINDER is CGA.

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Related Devices (Code: CGA)

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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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