FDA 510(k) Applications Submitted by DARRELL ALFORD
| 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. |
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