510(k) K872351

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

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