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FEMRX MORCELLATOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K963872
510(k) Type
Traditional
Applicant
GYNECARE INNOVATION CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1997
Days to Decision
113 days
Submission Type
Summary

FEMRX MORCELLATOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K963872
510(k) Type
Traditional
Applicant
GYNECARE INNOVATION CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1997
Days to Decision
113 days
Submission Type
Summary