FDA 510(k) Applications for Medical Device Product Code "HNC"
(Specula, Ophthalmic)

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


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