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ANTISERUM, HUMAN, IGA

Page Type
Cleared 510(K)
510(k) Number
K790703
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
4/12/1979
Days to Decision
0 days

ANTISERUM, HUMAN, IGA

Page Type
Cleared 510(K)
510(k) Number
K790703
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
4/12/1979
Days to Decision
0 days