Last synced on 14 November 2025 at 11:06 pm

ORTHO ABNORMAL COAGULATION LEVEL I/II

Page Type
Cleared 510(K)
510(k) Number
K832225
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
35 days

ORTHO ABNORMAL COAGULATION LEVEL I/II

Page Type
Cleared 510(K)
510(k) Number
K832225
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
35 days