HNW — Dilator, Lachrymal Class I
FDA Device Classification
Classification Details
- Product Code
- HNW
- Device Class
- Class I
- Regulation Number
- 886.4350
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K862070 | intermedics intraocular | INTER-SHARP | June 17, 1986 |
| K841002 | premier dental products | LACHRYMAL PROBES-VARIOUS | May 9, 1984 |
| K812097 | koi | KOI LACREMAL HOOK & DILATOR | August 18, 1981 |