Last synced on 14 November 2025 at 11:06 pm

FETAL HEMOGLOBIN

Page Type
Cleared 510(K)
510(k) Number
K892241
510(k) Type
Traditional
Applicant
SURE-TECH DIAGNOSTIC ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1989
Days to Decision
56 days

FETAL HEMOGLOBIN

Page Type
Cleared 510(K)
510(k) Number
K892241
510(k) Type
Traditional
Applicant
SURE-TECH DIAGNOSTIC ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1989
Days to Decision
56 days