Device Classification Name |
catheter, multiple lumen
|
510(k) Number |
K820446 |
Device Name |
CATHETER, MULTIPLE LUMEN |
Applicant |
DLP, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
DLP, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 878.4200
|
Classification Product Code |
|
Date Received | 02/18/1982 |
Decision Date | 03/11/1982 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|