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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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