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FDA 510(k) Applications Submitted by W. TIM MILLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K001410
05/04/2000
PHORESOR MODEL PM2000
IOMED, INC.
K001522
05/16/2000
TRANSQ3
IOMED, INC.
K974855
12/29/1997
PHORESOR II, MODEL PM900
IOMED, INC.
K982668
07/31/1998
PHORESOR II,MODEL PM900
IOMED, INC.
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