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TANDEM - HGH KIT

Page Type
Cleared 510(K)
510(k) Number
K821366
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1982
Days to Decision
31 days

TANDEM - HGH KIT

Page Type
Cleared 510(K)
510(k) Number
K821366
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1982
Days to Decision
31 days