PROVISO

Crown And Bridge, Temporary, Resin

SCIENTIFIC PHARMACEUTICALS, INC.

The following data is part of a premarket notification filed by Scientific Pharmaceuticals, Inc. with the FDA for Proviso.

Pre-market Notification Details

• Device ID: K041886
• 510k Number: K041886
• Device Name: PROVISO
• Classification: Crown And Bridge, Temporary, Resin
• Applicant: SCIENTIFIC PHARMACEUTICALS, INC. 3221 PRODUCER WAY Pomona, CA 91768 -3916
• Contact: Jan A Orlowski
• Correspondent: Jan A Orlowski; SCIENTIFIC PHARMACEUTICALS, INC. 3221 PRODUCER WAY Pomona, CA 91768 -3916
• Product Code: EBG
• CFR Regulation Number: 872.3770 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2004-07-12
• Decision Date: 2004-08-04

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00816526020381	K041886	000
D801SP58011N1	K041886	000
D801SP58012N1	K041886	000
D801SP580131	K041886	000
D801SP58013N1	K041886	000
D801SP58014N1	K041886	000
D801SP58015N1	K041886	000
D801SP58021	K041886	000
D801SP58031	K041886	000
D801SP58041	K041886	000
D801SP58051	K041886	000
00816526020336	K041886	000
00816526020343	K041886	000
00816526020350	K041886	000
00816526020367	K041886	000
00816526020374	K041886	000
D801SP58011	K041886	000