Device Classification Name |
catheter, intravascular, therapeutic, short-term less than 30 days
|
510(k) Number |
K022756 |
Device Name |
NIPRO BIO-FLEX CATHETER |
Applicant |
NIPRO MEDICAL CORP. |
1384 COPPERFIELD COURT |
LEXINGTON,
KY
40514 -1268
|
|
Applicant Contact |
KAELYN B HADLEY |
Correspondent |
NIPRO MEDICAL CORP. |
1384 COPPERFIELD COURT |
LEXINGTON,
KY
40514 -1268
|
|
Correspondent Contact |
KAELYN B HADLEY |
Regulation Number | 880.5200
|
Classification Product Code |
|
Date Received | 08/20/2002 |
Decision Date | 10/18/2002 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|