Stoeckert Instrumente
Stoeckert Instrumente holds FDA 510(k) medical device clearances, first cleared 1982, most recent 2001.
Top product codes for Stoeckert Instrumente
Recent clearances by Stoeckert Instrumente
- K002273 — STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE
- K001961 — STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE
- K002118 — STOCKERT COMPACT SYSTEM VERSION 2.0
- K992635 — INTERFACE MODULE IDDD
- K990512 — STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS
- K982014 — STOCKERT COMPACT SYSTEM
- K972321 — S3 MAST PUMP
- K971520 — S3 CYCLIC RPM CONTROL
- K962320 — S3 CARDIOPLEGIA CONTROL
- K955152 — STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER
- K955038 — STOCKERT S3 DOUBLE HEAD PUMP MODULE
- K950990 — STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE
- K812049 — STOCKERT CARDIAC PACING ELECTRODES
Data sourced from openFDA. This site is unofficial and independent of the FDA.