FDA 510(k) Applications for Medical Device Product Code "MCZ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K050656 | AMSINO INTERNATIONAL, INC. | AMSINO SUTURE REMOVAL KIT | 05/02/2005 |
K964827 | CONTINENTAL MEDICAL LABORATORIES, INC. | PROD. NO. 01-132 - SUTURE REMOVAL KIT | 02/14/1997 |
K963714 | GRAND MEDICAL PRODUCTS | GRAND MEDICAL SUTURE REMOVAL KIT | 11/27/1996 |