Bioject Medical Technologies, Inc.

Bioject Medical Technologies, Inc. holds 3 FDA 510(k) medical device clearances, first cleared 2004, most recent 2012.

Top product codes for Bioject Medical Technologies, Inc.

LHI — General Hospital2 devices
KZE — General Hospital1 device

Recent clearances by Bioject Medical Technologies, Inc.

K121270 — BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMCode KZE·2012-07-19
K043304 — Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01Code LHI·2005-01-14
K041564 — Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01Code LHI·2004-07-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.