Device Classification Name |
Catheter, Percutaneous, Neurovasculature
|
510(k) Number |
K242051 |
Device Name |
VersaD Delivery Catheter |
Applicant |
Unity Medical, Inc. |
6987 Washington Ave South |
Edina,
MN
55439
|
|
Applicant Contact |
Matthew Ogle |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Correspondent Contact |
Prithul Bom |
Regulation Number | 870.1250
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 07/12/2024 |
Decision Date | 01/17/2025 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Neurology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
|
|