Halt Medical, Inc. is one of 19088 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Halt Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACESSA GUIDANCE SYSTEM, ACESSA GUIDANCE HANDPIECE, THE ABLATION SYSTEM
4
Total
4
Cleared
0
Denied
Halt Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Brentwood, US.
Historical record: 4 cleared submissions from 2010 to 2014. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Halt Medical, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Halt Medical, Inc.
4 devices
Cleared
May 27, 2014
ACESSA GUIDANCE SYSTEM
Obstetrics & Gynecology
266d
Cleared
Apr 28, 2014
ACESSA GUIDANCE HANDPIECE
Obstetrics & Gynecology
287d
Cleared
CT
Nov 05, 2012
THE ABLATION SYSTEM
Obstetrics & Gynecology
132d
Cleared
Jun 14, 2010
HALT 2000GI ELECTROSURGICAL RF ABLATION SYSTEM MODEL HALT 2000GI
General & Plastic Surgery
168d