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FDA 510(k)

ACA GLUTAMYL TRANSFERASE

K-Number: K771800 · 1977-10-25

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1977-10-25
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA GLUTAMYL TRANSFERASE is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771800. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA GLUTAMYL TRANSFERASE?

ACA GLUTAMYL TRANSFERASE is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K771800.

When did ACA GLUTAMYL TRANSFERASE receive FDA 510(k) clearance?

ACA GLUTAMYL TRANSFERASE received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771800.

Who is the listed applicant for ACA GLUTAMYL TRANSFERASE?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACA GLUTAMYL TRANSFERASE?

The FDA product code for ACA GLUTAMYL TRANSFERASE is JJT.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. 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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Related Devices (Code: JJT)

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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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