Device Classification Name |
sterilizer, chemical
|
510(k) Number |
K190103 |
Device Name |
V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System, V-PRO 1 Plus Low Temperature Sterilization System, V-PRO 1 Low Temperature Sterilization System |
Applicant |
STERIS Corporation |
5960 Heisley Rd |
Mentor,
OH
44060
|
|
Applicant Contact |
Anthony Piotrkowski |
Correspondent |
STERIS Corporation |
5960 Heisley Rd |
Mentor,
OH
44060
|
|
Correspondent Contact |
Anthony Piotrkowski |
Regulation Number | 880.6860
|
Classification Product Code |
|
Date Received | 01/22/2019 |
Decision Date | 04/05/2019 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|