The following data is part of a premarket notification filed by Austenal Dental, Inc. with the FDA for Vitallium Wire.
Device ID | K872746 |
510k Number | K872746 |
Device Name: | VITALLIUM WIRE |
Classification | Clasp, Wire |
Applicant | AUSTENAL DENTAL, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
Contact | Gilbert K Ntow |
Correspondent | Gilbert K Ntow AUSTENAL DENTAL, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
Product Code | EJW |
CFR Regulation Number | 872.3285 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-07-13 |
Decision Date | 1987-07-21 |