Broncus Technologies, Inc. is one of 15029 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Broncus Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LUNGPOINT PLANNING AND VIRTUAL BRONCHOSCOPIC NAVIGATION (VBN) SOFTWARE, LUNGPOINT PROCEDURE PLANNING, LUNGPOINT VIRTUAL BRONCHOSCOPIC NAVIGATION VBN SYSTEM
11
Total
11
Cleared
0
Denied
Broncus Technologies, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 11 cleared submissions from 1998 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Broncus Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Broncus Technologies, Inc.
11 devices
Cleared
Oct 12, 2011
LUNGPOINT PLANNING AND VIRTUAL BRONCHOSCOPIC NAVIGATION (VBN) SOFTWARE
Radiology
86d
Cleared
Nov 17, 2009
LUNGPOINT PROCEDURE PLANNING
Radiology
14d
Cleared
May 05, 2009
LUNGPOINT VIRTUAL BRONCHOSCOPIC NAVIGATION VBN SYSTEM
Radiology
14d
Cleared
Apr 07, 2009
YIELD TISSUE SAMPLER
Ear, Nose, Throat
8d
Cleared
Apr 03, 2009
YIELD MINI DOPPLER SYSTEM
Radiology
14d
Cleared
Mar 13, 2009
LUNGPOINT VIRTUAL BRONCHOSCOPIC NAVIGATION VBN SYSTEM
Radiology
57d
Cleared
Oct 01, 2001
EXHALE PROBE
Radiology
13d
Cleared
May 08, 2001
EXHALE RF PROBE
Ear, Nose, Throat
12d
Cleared
Mar 20, 2001
EXHALE DOPPLER SYSTEM
Radiology
15d
Cleared
Jan 28, 2000
COAGULATION ELECTRODE, MODEL 2000
Ear, Nose, Throat
73d
Cleared
May 01, 1998
BRONCHIAL CATHETER SYSTEM
Ear, Nose, Throat
115d