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