The following data is part of a premarket notification filed by Heraeus Kulzer, Inc. with the FDA for Siloc System.
| Device ID | K970848 |
| 510k Number | K970848 |
| Device Name: | SILOC SYSTEM |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | HERAEUS KULZER, INC. 10005 MUIRLANDS BLVD. Irvine, CA 92718 -2595 |
| Contact | Sharon Parker |
| Correspondent | Sharon Parker HERAEUS KULZER, INC. 10005 MUIRLANDS BLVD. Irvine, CA 92718 -2595 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-03-07 |
| Decision Date | 1997-05-06 |