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FDA 510(k) Applications Submitted by GYNECARE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K992901
08/30/1999
GYNECARE VERSAPOINT G-VAP ELECTRODE
GYNECARE, INC.
K962482
06/26/1996
SCUBA SYSTEM
GYNECARE, INC.
K982738
08/06/1998
VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)
GYNECARE, INC.
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