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FDA 510(k)

SERUM, GLUTAMIC-OXALOACETIC

K-Number: K790017 · 1979-02-26

ApplicantFisher Scientific Co., LLC
Decision Date1979-02-26
Product CodeCIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERUM, GLUTAMIC-OXALOACETIC 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 1979-02-26 under 510(k) number K790017. The device is classified under product code CIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERUM, GLUTAMIC-OXALOACETIC?

SERUM, GLUTAMIC-OXALOACETIC is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K790017.

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

SERUM, GLUTAMIC-OXALOACETIC received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790017.

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

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-OXALOACETIC?

The FDA product code for SERUM, GLUTAMIC-OXALOACETIC is CIT.

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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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