H200 WIRELESS HAND REHABILITATION SYSTEM WITH OPTIONAL INTELLI-CONNECT EARPIECE TRIGGERING DEVICE— 510(k) K123636

Substantially Equivalent

Bioness, Inc.

FDA 510(k) clearance K123636 for H200 WIRELESS HAND REHABILITATION SYSTEM WITH OPTIONAL INTELLI-CONNECT EARPIECE TRIGGERING DEVICE, Substantially Equivalent on 2013-05-01. Applicant: Bioness, Inc..

Clearance details

Applicant: Bioness, Inc.
Product code: Code GZI
Advisory panel: Neurology
Date received: 2012-11-23
Decision date: 2013-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

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