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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