510(k) K872351

FIBERLASE II ND:YAG LASER FOR PULMONARY USE by Laser Media — Product Code LLO

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