HNL — Probe, Lachrymal Class I
FDA product code HNL covers "Probe, Lachrymal", a Class I medical device regulated under 21 CFR 886.4350. Submissions are reviewed by the Ophthalmic panel. At least 10 recent 510(k) clearances have been granted under this product code.
Classification details
- Product Code
- HNL
- Device Class
- Class I
- Regulation Number
- 886.4350
- Submission Type
- 510(k) Exempt
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K843491 | Concept | CONCEPT FIBER OPTIC CANALICULUS INTUBA | Oct 5, 1984 |
| K840861 | Hansen Ophthalmic Development Lab | TSE-ANDERSON MODIFIED LACRIMAL GROOV | May 9, 1984 |
| K833671 | Coopervision | STERILE OIL AND GUIDEWIRE | Jan 10, 1984 |
| K831901 | Visitec | LACIMAL INTUBATION SETS | Jul 12, 1983 |
| K813187 | Narco Scientific | PILLING LACRIMAL INTUBATION SYSTEM | Jan 28, 1982 |
| K812255 | Ethicon | ETHICON LACRIMAL STENT | Aug 20, 1981 |
| K802845 | Concept | CONCEPT CANALICULUS INTUBATION SET | Dec 17, 1980 |
| K801232 | Storz Instrument | JACKSON LACRIMAL INTUBATION SET | Jun 17, 1980 |
| K800089 | Jedmed Instrument | CRAWFORD LACRIMAL INTUBATION SET | Mar 3, 1980 |
| K770194 | Concept | NASO-LACRIMAL DUCT INSERT | Feb 14, 1977 |