Device Classification Name |
i.v. start kit
|
510(k) Number |
K930196 |
Device Name |
CEPTI-SEAL I.V. PREP KIT |
Applicant |
MEDI-FLEX HOSPITAL PRODUCTS, INC. |
8717 W. 110TH ST., SUITE 750 |
OVERLAND PARK,
KS
66210 -2103
|
|
Applicant Contact |
ORLANDO CORDOVA |
Correspondent |
MEDI-FLEX HOSPITAL PRODUCTS, INC. |
8717 W. 110TH ST., SUITE 750 |
OVERLAND PARK,
KS
66210 -2103
|
|
Correspondent Contact |
ORLANDO CORDOVA |
Regulation Number | 880.5200
|
Classification Product Code |
|
Date Received | 01/14/1993 |
Decision Date | 07/02/1993 |
Decision |
Substantially Equivalent - Kit With Drugs
(SEKD) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|