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 |