Disetronic Medical Systems AG
Disetronic Medical Systems AG holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2010.
Top product codes for Disetronic Medical Systems AG
Recent clearances by Disetronic Medical Systems AG
- K100704 — ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION DEVICE
- K070189 — ACCU-CHEK ULTRAFLEX INFUSION SET
- K063146 — ACCU-CHEK LINKASSIST
- K060876 — ACCU-CHEK INSULIN PUMP CONFIGURATION SOFTWARE (STANDARD), MODEL 04625137001
- K042887 — ACCU-CHEK SPIRIT
- K043000 — MODIFICATION TO D-TRONPLUS
- K033892 — ULTRAFLEX INFUSION SET
- K023471 — DISETRONIC H-TRONPLUS INSULIN INFUSION PUMP
- K022831 — MODIFICATION TO DISETRONIC D-TRONPLUS INSULIN INFUSION PUMP
- K021725 — DISETRONIC D-TRON INSULIN INFUSION PUMP
- K003977 — DISETRONIC RAPID SUBCUTANEOUS INFUSION SET AND DISTERONIC RAPID D SUBCUTANEOUS INFUSION SET
- K001629 — DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.