510(k) K974855

PHORESOR II, MODEL PM900 by Iomed, Inc. — Product Code KTB

Clearance Details

Decision
SN ()
Decision Date
March 27, 1998
Date Received
December 29, 1997
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