Device Classification Name |
device, percutaneous retrieval
|
510(k) Number |
K200268 |
Device Name |
Halo™ Single-Loop Snare Kit |
Applicant |
Argon Medical Devices, Inc. |
1445 Flat Creek Road |
Athens,
TX
75751
|
|
Applicant Contact |
Ana Jimenez-Hughes |
Correspondent |
Argon Medical Devices, Inc. |
1445 Flat Creek Road |
Athens,
TX
75751
|
|
Correspondent Contact |
Ana Jimenez-Hughes |
Regulation Number | 870.5150
|
Classification Product Code |
|
Date Received | 02/03/2020 |
Decision Date | 06/03/2020 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|