DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE
K-Number: K761090 · 1976-12-02
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Device Summary
Frequently Asked Questions
What is the DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE?
DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K761090.
When did DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE receive FDA 510(k) clearance?
DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761090.
Who is the listed applicant for DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE?
The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE?
The FDA product code for DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE is JQB.
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 Technicon Instruments Corp. 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.
Related Devices (Code: JQB)
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.
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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