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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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