Last synced on 29 September 2023 at 11:04 pm

T3(125) RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801843
510(k) Type
Traditional
Applicant
TECHNIA DIAGNOSTICS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1980
Days to Decision
46 days

T3(125) RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801843
510(k) Type
Traditional
Applicant
TECHNIA DIAGNOSTICS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1980
Days to Decision
46 days