510(k) K112133

OASYS SURGICAL LIGHT CONTROLLER by Oasys Healthcare — Product Code FTA

K112133 is an FDA 510(k) premarket notification submitted by Oasys Healthcare for the device "OASYS SURGICAL LIGHT CONTROLLER". The FDA issued a decision of Substantially Equivalent on March 1, 2012. The device falls under product code FTA (Light, Surgical, Accessories), a Class II device regulated under 21 CFR 878.4580.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 1, 2012
Date Received
July 26, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Light, Surgical, Accessories
Device Class
Class II
Regulation Number
878.4580
Review Panel
SU
Submission Type