PRECEDENT

Cement, Dental

RELIANCE ORTHODONTIC PRODUCTS, INC.

The following data is part of a premarket notification filed by Reliance Orthodontic Products, Inc. with the FDA for Precedent.

Pre-market Notification Details

• Device ID: K934405
• 510k Number: K934405
• Device Name: PRECEDENT
• Classification: Cement, Dental
• Applicant: RELIANCE ORTHODONTIC PRODUCTS, INC. P.O. BOX 678 Itasca, IL 60143
• Contact: Paul A Gange
• Correspondent: Paul A Gange; RELIANCE ORTHODONTIC PRODUCTS, INC. P.O. BOX 678 Itasca, IL 60143
• Product Code: EMA
• CFR Regulation Number: 872.3275 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-09-09
• Decision Date: 1994-01-21

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
D798PRS0	K934405	000
D798PRP150	K934405	000
D798PRP1000	K934405	000
D798PRL150	K934405	000
D798PRE0	K934405	000
D7981PRL300	K934405	000