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FDA 510(k) Applications Submitted by OAK CAROLINA, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981963
06/04/1998
SENSITEX EXAMINATION GLOVE
OAK CAROLINA, INC.
K981488
04/27/1998
GLOVE, OAKTEX EXAMINATION, GLOVE, PATIENT EXAMINATION
OAK CAROLINA, INC.
K952050
05/01/1995
GLOVE, EXAMINATION, VINYL
OAK CAROLINA, INC.
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