Product code HNL— Ophthalmic
CONCEPT CANALICULUS INTUBATION SET
- Classification name
- Probe, Lachrymal
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 10
- First cleared
- Most recent
Market context for product code HNL
FDA has cleared devices under product code HNL between 1977 and 1984, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1984
- 1983
- 1982
- 1981
- 1980
- 1977
Top applicants under product code HNL
Recent clearances under product code HNL
- K843491 — CONCEPT FIBER OPTIC CANALICULUS INTUBA
- K840861 — TSE-ANDERSON MODIFIED LACRIMAL GROOV
- K833671 — STERILE OIL AND GUIDEWIRE
- K831901 — LACIMAL INTUBATION SETS
- K813187 — PILLING LACRIMAL INTUBATION SYSTEM
- K812255 — ETHICON LACRIMAL STENT
- K802845 — CONCEPT CANALICULUS INTUBATION SET
- K801232 — JACKSON LACRIMAL INTUBATION SET
- K800089 — CRAWFORD LACRIMAL INTUBATION SET
- K770194 — NASO-LACRIMAL DUCT INSERT
Data sourced from openFDA. This site is unofficial and independent of the FDA.