Last synced on 14 November 2025 at 11:06 pm

TANDEM OTC HCG PREGNANCY TEST FOR CONSUMER USE

Page Type
Cleared 510(K)
510(k) Number
K863841
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1986
Days to Decision
82 days

TANDEM OTC HCG PREGNANCY TEST FOR CONSUMER USE

Page Type
Cleared 510(K)
510(k) Number
K863841
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1986
Days to Decision
82 days