510(k) K173349
K173349 is an FDA 510(k) premarket notification submitted by Toul Meditech AB for the device "Operio". The FDA issued a decision of Substantially Equivalent on December 20, 2017. The device falls under product code ORC (Air Filter Portable Apparatus), a Class II device regulated under 21 CFR 878.5070. Toul Meditech AB has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 2017
- Date Received
- October 25, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Air Filter Portable Apparatus
- Device Class
- Class II
- Regulation Number
- 878.5070
- Review Panel
- HO
- Submission Type
The sytem is intended to control the surgical environment to prevent bacterial contamination during surgical procedures.