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DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K761090
510(k) Type
Traditional
Applicant
TECHNICON INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1976
Days to Decision
10 days

DIAGNOSTIC METHOD-8-GLUTAMYLTRANSFERASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K761090
510(k) Type
Traditional
Applicant
TECHNICON INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1976
Days to Decision
10 days