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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