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FEMRX OPERASTAR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954648
510(k) Type
Traditional
Applicant
GYNECARE INNOVATION CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1996
Days to Decision
156 days
Submission Type
Statement

FEMRX OPERASTAR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954648
510(k) Type
Traditional
Applicant
GYNECARE INNOVATION CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1996
Days to Decision
156 days
Submission Type
Statement