FDA 510(k) Applications Submitted by SUMMIT GLOVE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093516 | 11/13/2009 | NITRITECH OR MULTIPLE PRIVATE LABEL NON STERILE POWDERED NITRILE EXAMINATION GLOVES | SUMMIT GLOVE, INC. |
| K093517 | 11/13/2009 | NITRITECH OR MULTIPLE PRIVATE LABEL NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVE | SUMMIT GLOVE, INC. |
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