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Osypka Medical, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K123916	PSA SERIES	DTE	2013-04-09	View
510(k)	K082242	ICON, MODEL C3	DSB	2008-10-08	View
510(k)	K081035	AESCULON C2, AESCULON CHF CLINIC C2, AESCULON HYPERTENSION CLINIC C2 AND AESCULON PACEMAKER CLINIC C2	DSB	2008-05-30	View
510(k)	K070985	AESCULON CHF, HYPERTENSION & PACEMAKER CLINIC	DSB	2008-02-01	View
510(k)	K033130	PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOR	DTE	2003-10-31	View
510(k)	K022939	OSCOR PACE 101/101H AND ACCESSORIES, ST.JUDE MEDICAL MODEL 3077 AND ACCESSORIES,CARDIOTRONIC PACE 101 AND ACCESSORIES	DTE	2002-10-03	View
510(k)	K020896	OSCOR PACE 203/PACE 203H DUAL-CHAMBER TEMPORARY PACEMAKER, ST. JUDE MEDICAL, MODEL 3085 DUAL-CHAMBER EXTERNAL PULSE GENE	DTE	2002-06-14	View

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