The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Fluor Protector.
Device ID | K946032 |
510k Number | K946032 |
Device Name: | FLUOR PROTECTOR |
Classification | Varnish, Cavity |
Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Contact | Lloyd V Ziemendorf |
Correspondent | Lloyd V Ziemendorf IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Product Code | LBH |
CFR Regulation Number | 872.3260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-12-09 |
Decision Date | 1995-03-07 |