| ||||||||||||||
FDA 510(k) Applications for Medical Device Product Code "HIO"
|
||||||||||||||
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K955679 | CONTOUR FABRICATORS OF FLORIDA, INC. | RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAY | 03/12/1996 |
| K960203 | GE MEDICAL SYSTEMS | G.E. STERILE AMNIOCENTESIS TRAY | 03/14/1996 |