The following data is part of a premarket notification filed by Gc America, Inc. with the FDA for Exa Bite Registration Material.
| Device ID | K933206 |
| 510k Number | K933206 |
| Device Name: | EXA BITE REGISTRATION MATERIAL |
| Classification | Material, Impression |
| Applicant | GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
| Contact | Terry L Joritz |
| Correspondent | Terry L Joritz GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-01 |
| Decision Date | 1993-09-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10386040004978 | K933206 | 000 |
| 10386040004961 | K933206 | 000 |
| 14548161333740 | K933206 | 000 |