ILLUSION

Material, Tooth Shade, Resin

BISCO, INC.

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

Pre-market Notification Details

• Device ID: K993192
• 510k Number: K993192
• Device Name: ILLUSION
• Classification: Material, Tooth Shade, Resin
• Applicant: BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193
• Contact: Katheyn B Patterson
• Correspondent: Katheyn B Patterson; BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193
• Product Code: EBF
• CFR Regulation Number: 872.3690 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1999-08-24
• Decision Date: 1999-10-27
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
D757C412D20	K993192	000
00810111540674	K993192	000
00810111540636	K993192	000
00810111540650	K993192	000
00810111540711	K993192	000
00810111540735	K993192	000
00810111540759	K993192	000
00810111540773	K993192	000
D757C412A10	K993192	000
D757C412A20	K993192	000
D757C412A30	K993192	000
D757C412B10	K993192	000
D757C412MB0	K993192	000
D757C412MO0	K993192	000
D757C412OP0	K993192	000
D757C412TR0	K993192	000
D757C412C20	K993192	000
00810111540698	K993192	000