510(k) K872351
K872351 is an FDA 510(k) premarket notification submitted by Laser Media for the device "FIBERLASE II ND:YAG LASER FOR PULMONARY USE". The FDA issued a decision of Substantially Equivalent on December 11, 1987. The device falls under product code LLO (Laser, Neodymium:Yag, Pulmonary Surgery), a Class II device regulated under 21 CFR 874.4500. Laser Media has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 11, 1987
- Date Received
- June 17, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laser, Neodymium:Yag, Pulmonary Surgery
- Device Class
- Class II
- Regulation Number
- 874.4500
- Review Panel
- AN
- Submission Type