510(k) K010388

SONDREX P.A.L. SYSTEM by Ohmeda Medical — Product Code HCC

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