DZS — Capsule, Dental, Amalgam Class I
FDA Device Classification
Classification Details
- Product Code
- DZS
- Device Class
- Class I
- Regulation Number
- 872.3110
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K822610 | syntex dental products | PRECAPSULED DENTAL AMALGAM | September 14, 1982 |
| K802967 | johnson and johnson professionals | DISPERSALLOY-DISPERSED PHASE ALLOY SELF- | December 30, 1980 |
| K781243 | lee pharmaceuticals | MERCURY DISP. CAPSULE | September 20, 1978 |
| K780966 | lee pharmaceuticals | LEE-ALLOY DISPOSABLE CAPSULES | August 21, 1978 |