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Oak Carolina, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K981963 SENSITEX EXAMINATION GLOVELYZ1998-07-24 View
510(k) K981488 GLOVE, OAKTEX EXAMINATION, GLOVE, PATIENT EXAMINATIONLYZ1998-07-07 View
510(k) K952050 GLOVE, EXAMINATION, VINYLLYZ1996-08-12 View
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