The following data is part of a premarket notification filed by Aalba Dent, Inc. with the FDA for Verasoft Es.
| Device ID | K033356 |
| 510k Number | K033356 |
| Device Name: | VERASOFT ES |
| Classification | Alloy, Metal, Base |
| Applicant | AALBA DENT, INC. 400 WATT DR. Cordelia, CA 94534 |
| Contact | Vincent Benetti |
| Correspondent | Vincent Benetti AALBA DENT, INC. 400 WATT DR. Cordelia, CA 94534 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-20 |
| Decision Date | 2003-12-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 90852187007111 | K033356 | 000 |