510(k) K954126

TRANSQ ELECTRODE PHORESOR II by Iomed, Inc. — Product Code KTB

K954126 is an FDA 510(k) premarket notification submitted by Iomed, Inc. for the device "TRANSQ ELECTRODE PHORESOR II". The FDA issued a decision of SN on January 19, 1996. The device falls under product code KTB (Device, Iontophoresis, Specific Uses), a Class II device regulated under 21 CFR 890.5525. Iomed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
January 19, 1996
Date Received
September 1, 1995
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