B&B Medical Technologies, Inc.
B&B Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2004.
Top product codes for B&B Medical Technologies, Inc.
Recent clearances by B&B Medical Technologies, Inc.
- K030396 — OMNI~NEB; OMNI~MAX
- K980407 — HOPE NEBULIZER
- K960663 — UNIVERSAL BITE BLOCK
- K945816 — QUICK-LOCK
- K944324 — SURE-LOCK VENTILATOR TUBING HOLDER
- K935171 — STABILTRACH
- K925386 — ADHESIVE E.T. TAPE
- K923690 — MINI HEART
- K913015 — HEART NEBULIZER FLOWMETER ADAPTOR
- K913753 — BODAI NEO2 -SAFE AIRWAY PRESSURE CAP
- K913000 — HEART NEBULIZER POLE CLAMP
- K912884 — E.T. TAPE II
- K900912 — BABY E.T. TAPE II
- K902065 — E.T. TAPE II
- K900228 — H.E.A.R.T. NEBULIZER
- K900787 — NASAL E.T. TAPE
- K881849 — BODAI M.D.D. ADAPTOR(TM)
- K873696 — BODAI NEO2-SAFE(TM)
- K873491 — BLOCK, BITE, INTUBATION
- K871560 — BABY E.T. TAPE(TM)
- K863510 — OXY-OFF(TM)
- K863653 — SUCTION-OFF
- K862084 — E. T. TAPE ENDOTRACHEAL TUBE HOLDER
Data sourced from openFDA. This site is unofficial and independent of the FDA.