Emcision , Ltd. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Emcision , Ltd. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in London, GB.
Historical record: 10 cleared submissions from 2005 to 2018.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Emcision , Ltd.
10 devices
Cleared
Mar 20, 2018
Habib EndoHPB
Gastroenterology & Urology
57d
Cleared
Jul 07, 2016
Habib EUS RFA
General & Plastic Surgery
58d
Cleared
Jun 24, 2015
Habib EUS RFA
General & Plastic Surgery
167d
Cleared
Jun 10, 2009
HABIB ENDOHPB
Gastroenterology & Urology
212d
Cleared
Mar 27, 2008
HABIB HEXABLATE 10
General & Plastic Surgery
14d
Cleared
Jan 09, 2008
HABIB LAPAROSCOPIC HEXABLATE
General & Plastic Surgery
12d
Cleared
Nov 29, 2007
HABIB ENDOBLATE
Gastroenterology & Urology
97d
Cleared
Oct 02, 2007
HABIB VESEAL
General & Plastic Surgery
61d
Cleared
Jun 27, 2007
HABIB HEXABLATE
General & Plastic Surgery
69d
Cleared
Aug 15, 2005
HABIB 4X
General & Plastic Surgery
75d