Medical Device Manufacturer · US , Orangevale , CA

B&B Medical Technologies, Inc. - FDA 510(k) Cleared Devices

23 submissions · 22 cleared · Since 1986

Total

Cleared

Denied

B&B Medical Technologies, Inc. has 22 FDA 510(k) cleared anesthesiology devices. Based in Orangevale, US.

Historical record: 22 cleared submissions from 1986 to 2004.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - B&B Medical Technologies, Inc.

23 devices

1-23 of 23

Cleared May 07, 2004

OMNI~NEB

K030396 · CAF

Anesthesiology · 456d

Cleared May 27, 1998

HOPE NEBULIZER

K980407 · CAF

Anesthesiology · 113d

SURE-LOCK VENTILATOR TUBING HOLDER

Anesthesiology · 175d

HEART NEBULIZER FLOWMETER ADAPTOR

K913015 · CAF

Anesthesiology · 135d

Cleared Oct 23, 1991

BODAI NEO2 -SAFE AIRWAY PRESSURE CAP

K913753 · CAI

Anesthesiology · 63d

Cleared Aug 02, 1991

HEART NEBULIZER POLE CLAMP

Anesthesiology · 157d

BODAI M.D.D. ADAPTOR(TM)

Anesthesiology · 213d

Cleared Oct 20, 1987

BLOCK, BITE, INTUBATION

General & Plastic Surgery · 19d

Cleared Jun 05, 1986

E. T. TAPE ENDOTRACHEAL TUBE HOLDER

K862084 · CBH

Anesthesiology · 3d

B&B Medical Technologies, Inc. - FDA 510(k) Cleared Devices

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