Last synced on 14 November 2025 at 11:06 pm

TESTOSTERONE RADIOIMMUNOASSY KIT

Page Type
Cleared 510(K)
510(k) Number
K802135
510(k) Type
Traditional
Applicant
RADIOIMMUNOASSAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1980
Days to Decision
36 days

TESTOSTERONE RADIOIMMUNOASSY KIT

Page Type
Cleared 510(K)
510(k) Number
K802135
510(k) Type
Traditional
Applicant
RADIOIMMUNOASSAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1980
Days to Decision
36 days