Medical Device Manufacturer · US , Orangevale , CA

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

23 submissions · 22 cleared · Since 1986

Recent clearances: OMNI~NEB, HOPE NEBULIZER, UNIVERSAL BITE BLOCK

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.

B&B Medical Technologies, Inc. is one of 5576 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

23 devices

1-12 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

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

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

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