The following data is part of a premarket notification filed by Ultradent Products, Inc. with the FDA for Permaquik Bonding Primer.
Device ID | K951867 |
510k Number | K951867 |
Device Name: | PERMAQUIK BONDING PRIMER |
Classification | Agent, Tooth Bonding, Resin |
Applicant | ULTRADENT PRODUCTS, INC. 505 WEST 10200 SOUTH South Jordan, UT 84095 |
Contact | L. M Chatwin |
Correspondent | L. M Chatwin ULTRADENT PRODUCTS, INC. 505 WEST 10200 SOUTH South Jordan, UT 84095 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-04-21 |
Decision Date | 1995-05-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00883205104205 | K951867 | 000 |
00883205103680 | K951867 | 000 |