510(k) K001522

TRANSQ3 by Iomed, Inc. — Product Code KTB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 18, 2000
Date Received
May 16, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Iontophoresis, Specific Uses
Device Class
Class II
Regulation Number
890.5525
Review Panel
PM
Submission Type