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PREGNOSPIA II

Page Type
Cleared 510(K)
510(k) Number
K881435
510(k) Type
Traditional
Applicant
ORGANON TEKNIKA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1988
Days to Decision
52 days

PREGNOSPIA II

Page Type
Cleared 510(K)
510(k) Number
K881435
510(k) Type
Traditional
Applicant
ORGANON TEKNIKA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1988
Days to Decision
52 days