The following data is part of a premarket notification filed by 3m Espe Ag Dental Products with the FDA for Hermes Bond.
| Device ID | K033974 |
| 510k Number | K033974 |
| Device Name: | HERMES BOND |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | 3M ESPE AG DENTAL PRODUCTS ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
| Contact | Andreas Petermann |
| Correspondent | Andreas Petermann 3M ESPE AG DENTAL PRODUCTS ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-22 |
| Decision Date | 2004-02-06 |
| Summary: | summary |