Last synced on 27 January 2023 at 11:04 pm

T4 RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802469
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
34 days

T4 RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802469
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
34 days