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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact