510(k) K812255
K812255 is an FDA 510(k) premarket notification submitted by ETHICON, Inc. for the device "ETHICON LACRIMAL STENT". The FDA issued a decision of Substantially Equivalent on Aug 20, 1981. The device falls under product code HNL (Probe, Lachrymal), a Class I device regulated under 21 CFR 886.4350. ETHICON, Inc. has 207 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 20, 1981
- Date Received
- Aug 12, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Probe, Lachrymal
- Device Class
- Class I
- Regulation Number
- 886.4350
- Review Panel
- OP
- Submission Type
- 510(k) Exempt