510(k) K010388
K010388 is an FDA 510(k) premarket notification submitted by Ohmeda Medical for the device "SONDREX P.A.L. SYSTEM". The FDA issued a decision of Substantially Equivalent on December 11, 2001. The device falls under product code HCC (Device, Biofeedback), a Class II device regulated under 21 CFR 882.5050. Ohmeda Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 11, 2001
- Date Received
- February 8, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Biofeedback
- Device Class
- Class II
- Regulation Number
- 882.5050
- Review Panel
- NE
- Submission Type