The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Gly-etch.
Device ID | K961190 |
510k Number | K961190 |
Device Name: | GLY-ETCH |
Classification | Sealant, Pit And Fissure, And Conditioner |
Applicant | CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
Contact | John Discko |
Correspondent | John Discko CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
Product Code | EBC |
CFR Regulation Number | 872.3765 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-03-26 |
Decision Date | 1996-04-23 |