PRO-V

Crown And Bridge, Temporary, Resin

BISCO, INC.

The following data is part of a premarket notification filed by Bisco, Inc. with the FDA for Pro-v.

Pre-market Notification Details

• Device ID: K073263
• 510k Number: K073263
• Device Name: PRO-V
• Classification: Crown And Bridge, Temporary, Resin
• Applicant: BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193
• Contact: Benjamin Lichtenwalner
• Correspondent: Benjamin Lichtenwalner; BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193
• Product Code: EBG
• CFR Regulation Number: 872.3770 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2007-11-20
• Decision Date: 2008-02-14
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
D757H40010	K073263	000