FDA 510(k) Applications for Medical Device Product Code "NLL"
(Staple, Implantable, Reprocessed)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K033578 | CLEAR MEDICAL, INC. | REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS | 07/11/2005 |
| K070930 | STERILMED, INC. | REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS | 10/18/2007 |
| K070859 | STERILMED, INC. | REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS | 09/12/2007 |
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