The following data is part of a premarket notification filed by Vident with the FDA for Vident 500 Alloy And Vident 550 Be Alloy.
| Device ID | K932893 |
| 510k Number | K932893 |
| Device Name: | VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY |
| Classification | Alloy, Metal, Base |
| Applicant | VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Contact | Ray E Morrow |
| Correspondent | Ray E Morrow VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-10 |
| Decision Date | 1994-03-28 |