Last synced on 14 November 2025 at 11:06 pm

LEAP RHEUMATOID FACTOR TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831941
510(k) Type
Traditional
Applicant
COOPER DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
32 days

LEAP RHEUMATOID FACTOR TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831941
510(k) Type
Traditional
Applicant
COOPER DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
32 days