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THYROSCREEN TM T4 DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K770474
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1977
Days to Decision
48 days

THYROSCREEN TM T4 DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K770474
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1977
Days to Decision
48 days