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TERUMO SENSIBEAD EIA PROGESTERONE KIT

Page Type
Cleared 510(K)
510(k) Number
K881693
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1988
Days to Decision
49 days

TERUMO SENSIBEAD EIA PROGESTERONE KIT

Page Type
Cleared 510(K)
510(k) Number
K881693
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1988
Days to Decision
49 days