FDA 510(k) Applications Submitted by OSYPKA MEDICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K070985 |
04/06/2007 |
AESCULON CHF, HYPERTENSION & PACEMAKER CLINIC |
OSYPKA MEDICAL, INC. |
| K081035 |
04/11/2008 |
AESCULON C2, AESCULON CHF CLINIC C2, AESCULON HYPERTENSION CLINIC C2 AND AESCULON PACEMAKER CLINIC C2 |
OSYPKA MEDICAL, INC. |
| K082242 |
08/07/2008 |
ICON, MODEL C3 |
OSYPKA MEDICAL, INC. |
| K123916 |
12/19/2012 |
PSA SERIES |
OSYPKA MEDICAL, INC. |
| K020896 |
03/19/2002 |
OSCOR PACE 203/PACE 203H DUAL-CHAMBER TEMPORARY PACEMAKER, ST. JUDE MEDICAL, MODEL 3085 DUAL-CHAMBER EXTERNAL PULSE GENE |
OSYPKA MEDICAL, INC. |
| K022939 |
09/04/2002 |
OSCOR PACE 101/101H AND ACCESSORIES, ST.JUDE MEDICAL MODEL 3077 AND ACCESSORIES,CARDIOTRONIC PACE 101 AND ACCESSORIES |
OSYPKA MEDICAL, INC. |
| K033130 |
09/30/2003 |
PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOR |
OSYPKA MEDICAL, INC. |
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