Last synced on 14 November 2025 at 11:06 pm

ANTI-GLOBULIN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K792695
510(k) Type
Traditional
Applicant
MERIDIAN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1980
Days to Decision
28 days

ANTI-GLOBULIN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K792695
510(k) Type
Traditional
Applicant
MERIDIAN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1980
Days to Decision
28 days