Device Classification Name |
Indicator, Physical/Chemical Sterilization Process
|
510(k) Number |
K003533 |
Device Name |
CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L |
Applicant |
STERITEC PRODUCTS, INC. |
599 TOPEKA WAY, SUITE 700 |
CASTLE ROCK,
CO
80104
|
|
Applicant Contact |
LINDA NELSON |
Correspondent |
STERITEC PRODUCTS, INC. |
599 TOPEKA WAY, SUITE 700 |
CASTLE ROCK,
CO
80104
|
|
Correspondent Contact |
LINDA NELSON |
Regulation Number | 880.2800
|
Classification Product Code |
|
Date Received | 11/16/2000 |
Decision Date | 02/07/2001 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Abbreviated
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|