HMM — Distometer Class I
FDA Device Classification
Classification Details
- Product Code
- HMM
- Device Class
- Class I
- Regulation Number
- 886.1190
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K882575 | hagg-streit service | DISTOMETER | July 1, 1988 |
| K873440 | allegheny plastics | RULE, PUPILLARY | September 21, 1987 |