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FDA 510(k)

GLUTAMATE OXALACETIC TRANSAMINASE

K-Number: K770917 · 1977-07-14

Decision Date1977-07-14
Product Code
DecisionSubstantially Equivalent

Device Summary

GLUTAMATE OXALACETIC TRANSAMINASE is the device name listed in this FDA 510(k) record. The listed applicant is The Dow Chemical Co.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K770917. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUTAMATE OXALACETIC TRANSAMINASE?

GLUTAMATE OXALACETIC TRANSAMINASE is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is The Dow Chemical Co.. The 510(k) number is K770917.

When did GLUTAMATE OXALACETIC TRANSAMINASE receive FDA 510(k) clearance?

GLUTAMATE OXALACETIC TRANSAMINASE received FDA 510(k) clearance on 1977-07-14, under 510(k) number K770917.

Who is the listed applicant for GLUTAMATE OXALACETIC TRANSAMINASE?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing The Dow Chemical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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