VCARE

Cannula, Manipulator/injector, Uterine

CONMED CORPORATION

The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Vcare.

Pre-market Notification Details

• Device ID: K142716
• 510k Number: K142716
• Device Name: VCARE
• Classification: Cannula, Manipulator/injector, Uterine
• Applicant: CONMED CORPORATION 525 FRENCH ROAD Utica, NY 13502
• Contact: Anna D'lima
• Correspondent: Anna D'lima; CONMED CORPORATION 525 FRENCH ROAD Utica, NY 13502
• Product Code: LKF
• CFR Regulation Number: 884.4530 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2014-09-23
• Decision Date: 2015-02-10
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20653405082092	K142716	000
20653405082085	K142716	000
20653405082078	K142716	000
20653405082061	K142716	000
20653405003813	K142716	000
20653405003806	K142716	000
20653405003790	K142716	000
10653405003748	K142716	000