510(k) K110422
K110422 is an FDA 510(k) premarket notification submitted by Technomed Europe for the device "SURGICAL STIMULATORS". The FDA issued a decision of Substantially Equivalent on May 26, 2011. The device falls under product code ETN (Stimulator, Nerve), a Class II device regulated under 21 CFR 874.1820. Technomed Europe has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 26, 2011
- Date Received
- February 14, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Nerve
- Device Class
- Class II
- Regulation Number
- 874.1820
- Review Panel
- EN
- Submission Type