FDA 510(k) Applications for Medical Device Product Code "EXI"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K963950 | BIODERM, INC. | BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE | 01/10/1997 |
K970443 | HOLLISTER, INC. | HOLLISTER RETRACTED PENIS POUCH | 02/25/1997 |
K971499 | MEDIQUEST, INC. | FEMALE EXTERNAL URINARY COLLECTION POUCH | 08/28/1997 |