510(k) K112133
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