FDA 510(k) Applications Submitted by BRADLEY L PUGH

FDA 510(k) Number Submission Date Device Name Applicant
K000421 02/08/2000 BIOGEL NEOTECH II POWDER-FREE NEOPRENE SURGEON'S GLOVE SSL AMERICAS, INC. (REGENT MEDICAL)
K991677 05/17/1999 REGENT SKINDENDE EXAM GLOVE, REGENT BIOGEL D, REGENTBIOGEL DIAGNOSTIC (POWDERFREE) LONDON INTERNATIONAL GROUP, INC.


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