Osypka Medical, Inc. is one of 19620 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osypka Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PSA SERIES, ICON, MODEL C3, AESCULON C2, AESCULON CHF CLINIC C2, AESCULON HYPERTENSION CLINIC C2 AND AESCULON PACEMAKER CLINIC C2
7
Total
6
Cleared
0
Denied
Osypka Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Historical record: 6 cleared submissions from 2002 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Osypka Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osypka Medical, Inc.
7 devices
Cleared
Apr 09, 2013
PSA SERIES
Cardiovascular
111d
Cleared
Oct 08, 2008
ICON, MODEL C3
Cardiovascular
62d
Cleared
May 30, 2008
AESCULON C2, AESCULON CHF CLINIC C2, AESCULON HYPERTENSION CLINIC C2 AND...
Cardiovascular
49d
Cleared
Feb 01, 2008
AESCULON CHF, HYPERTENSION & PACEMAKER CLINIC
Cardiovascular
301d
Cleared
Oct 31, 2003
PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOR
Cardiovascular
31d
Cleared
Oct 03, 2002
OSCOR PACE 101/101H AND ACCESSORIES, ST.JUDE MEDICAL MODEL 3077 AND...
Cardiovascular
29d
Cleared
Jun 14, 2002
OSCOR PACE 203/PACE 203H DUAL-CHAMBER TEMPORARY PACEMAKER, ST. JUDE MEDICAL,...
Cardiovascular
87d