Andronic Devices, Ltd.
Andronic Devices, Ltd. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 1994.
Top product codes for Andronic Devices, Ltd.
Recent clearances by Andronic Devices, Ltd.
- K940812 — INSIGHT ELECTRONIC ALIGNMENT INDICATOR
- K934926 — INSITE MODEL 20 & MODEL 15 INSUFFLATORS
- K934928 — INSITE FILTER & TUBING SET
- K935381 — KAPS POSITIONING ARM
- K934124 — AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM
- K936308 — ENDEX ENDOSCOPIC POSITIONING SYSTEM
- K932253 — ARTHROBOT BI-FOLD DRAPE
- K922625 — ADEPT ENDOSCOPIC POSITIONER
- K922626 — ADEPT INSTRUMENT POSITIONING ACCESSORY
- K911520 — ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE
- K911521 — ARTHROBOT(TM) 96 (240 CM) DRAPE WITH 1 STRAP
- K911522 — ARTHROBOT(TM) WRIST HOLDER ACCESSORY
- K880227 — ARTHROBOT(TM) LOWER LIMB POSITIONER
- K874762 — ARTHROTRACT UPPER LIMB TRACTION ACCESSORY
- K873079 — ARTHROBOT 100 UPPER LIMB POSITIONER
- K873080 — ARTHROBOT 101 UPPER LIMB TRACTION ACCESSORY
Data sourced from openFDA. This site is unofficial and independent of the FDA.