The following data is part of a premarket notification filed by Heraeus Kulzer, Inc. with the FDA for Gluma Comfort Bond + Desensitizer.
| Device ID | K992292 |
| 510k Number | K992292 |
| Device Name: | GLUMA COMFORT BOND + DESENSITIZER |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 |
| Contact | Cheryl V Zimmerman |
| Correspondent | Cheryl V Zimmerman HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-07 |
| Decision Date | 1999-10-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| J014660182220 | K992292 | 000 |
| J014660056640 | K992292 | 000 |
| J014660017100 | K992292 | 000 |