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FDA 510(k)

SERUM, GLUTAMIC-PYRUVIC

K-Number: K790016 · 1979-02-15

ApplicantFisher Scientific Co., LLC
Decision Date1979-02-15
Product CodeCKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERUM, GLUTAMIC-PYRUVIC is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1979-02-15 under 510(k) number K790016. The device is classified under product code CKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERUM, GLUTAMIC-PYRUVIC?

SERUM, GLUTAMIC-PYRUVIC is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K790016.

When did SERUM, GLUTAMIC-PYRUVIC receive FDA 510(k) clearance?

SERUM, GLUTAMIC-PYRUVIC received FDA 510(k) clearance on 1979-02-15, under 510(k) number K790016.

Who is the listed applicant for SERUM, GLUTAMIC-PYRUVIC?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERUM, GLUTAMIC-PYRUVIC?

The FDA product code for SERUM, GLUTAMIC-PYRUVIC is CKA.

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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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