FDA 510(k) Applications Submitted by APOLLO ENDOSURGERY, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
DEN210045 |
09/30/2021 |
APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System |
Apollo Endosurgery, Inc. |
K081853 |
06/30/2008 |
OVERSTITCH ENDOSCOPIC SUTURE SYSTEM |
APOLLO ENDOSURGERY, INC. |
K082102 |
07/25/2008 |
GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00 |
APOLLO ENDOSURGERY, INC. |
K082114 |
07/28/2008 |
ELECTROCAUTERY DILATION BALLOON, MODELS: EDB-0018-00, EDB-0020-00, EDB-0022-00 |
APOLLO ENDOSURGERY, INC. |
K090583 |
03/04/2009 |
ENDOSCOPIC MONOPOLAR SCISSORS, MODELS EMS-235, EMS-165 |
APOLLO ENDOSURGERY, INC. |
K103155 |
10/26/2010 |
SUMO ACCESS AND TISSUE RESECTION SYSTEM |
APOLLO ENDOSURGERY, INC. |
K122270 |
07/30/2012 |
OVERTUBE ENDOSCOPIC ACCESS SYSTEM |
APOLLO ENDOSURGERY, INC. |
K201808 |
07/01/2020 |
X-Tack Endoscopic HeliX Tacking System |
Apollo Endosurgery, Inc. |
|
|