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Calliope Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K840063	CATAREX VITRECUTTER I/A DISPOS. CUT	HQC	1984-10-05	View
510(k)	K840181	CATAREX/ULTRASONICS KIT	HQC	1984-10-05	View
510(k)	K832446	CATAREX DIAP. EXTRACAPSULAR CATARACT	HQE	1983-10-19	View

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