FDA 510(k) Applications for Medical Device Product Code "MKY"
(System, Skin Closure)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K962144 | PHOENIX BIOMEDICAL CORP. | PHOENIX ETE TISSUE EXTENSION SYSTEM | 01/14/1997 |
| K970439 | PROGRESSIVE SURGICAL PRODUCTS, INC. | PROXIDERM (D-460,D 90 460,D 180,460, PS 460) | 04/16/1997 |
| K982439 | PROGRESSIVE SURGICAL PRODUCTS, INC. | PROXIDERM, MODELS TN 460, TN 90 460, BK 460 | 09/08/1998 |
| K002315 | WISEBANDS LTD. | WISEBANDS SKIN CLOSURE DEVICE | 03/15/2001 |
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