The following data is part of a premarket notification filed by Sybron Dental Specialties, Inc. with the FDA for Quantec-e Endo System.
| Device ID | K990739 |
| 510k Number | K990739 |
| Device Name: | QUANTEC-E ENDO SYSTEM |
| Classification | Handpiece, Direct Drive, Ac-powered |
| Applicant | SYBRON DENTAL SPECIALTIES, INC. 1717 WEST COLLINS AVE. Orange, CA 92867 |
| Contact | Colleen Boswell |
| Correspondent | Colleen Boswell SYBRON DENTAL SPECIALTIES, INC. 1717 WEST COLLINS AVE. Orange, CA 92867 |
| Product Code | EKX |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-05 |
| Decision Date | 1999-05-26 |
| Summary: | summary |