Osypka Medical, Inc.
Osypka Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2013.
Top product codes for Osypka Medical, Inc.
Recent clearances by Osypka Medical, Inc.
- K123916 — PSA SERIES
- K082242 — ICON, MODEL C3
- K081035 — AESCULON C2, AESCULON CHF CLINIC C2, AESCULON HYPERTENSION CLINIC C2 AND AESCULON PACEMAKER CLINIC C2
- K070985 — AESCULON CHF, HYPERTENSION & PACEMAKER CLINIC
- K033130 — PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOR
- K022939 — OSCOR PACE 101/101H AND ACCESSORIES, ST.JUDE MEDICAL MODEL 3077 AND ACCESSORIES,CARDIOTRONIC PACE 101 AND ACCESSORIES
- K020896 — OSCOR PACE 203/PACE 203H DUAL-CHAMBER TEMPORARY PACEMAKER, ST. JUDE MEDICAL, MODEL 3085 DUAL-CHAMBER EXTERNAL PULSE GENE
Data sourced from openFDA. This site is unofficial and independent of the FDA.