FDA 510(k) Applications Submitted by LONDON INTERNATIONAL GROUP, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K991677 05/17/1999 REGENT SKINDENDE EXAM GLOVE, REGENT BIOGEL D, REGENTBIOGEL DIAGNOSTIC (POWDERFREE) LONDON INTERNATIONAL GROUP, INC.
K980942 03/12/1998 REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE LONDON INTERNATIONAL GROUP, INC.
K971514 04/25/1997 REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE LONDON INTERNATIONAL GROUP, INC.
K984249 11/30/1998 SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE LONDON INTERNATIONAL GROUP, INC.
K980516 02/10/1998 REGENT BIOGEL ORTHOPEDIC SURGICAL GLOVE LONDON INTERNATIONAL GROUP, INC.


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