Last synced on 14 November 2025 at 11:06 pm

PROGESTERONE CLASP RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K871211
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1987
Days to Decision
18 days

PROGESTERONE CLASP RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K871211
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1987
Days to Decision
18 days