FDA 510(k) Applications for Medical Device Product Code "HNC"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K964289 | EYEFIX, INC. | EYE FIXATION SPECULUM | 12/17/1996 |
K981235 | LASER CENTER DEV. CORP. | OCULOSTAT | 07/15/1998 |
K022836 | STEPHENS INSTRUMENTS | STEPHENS DISPOSABLE SPECULUM | 11/01/2002 |