Device Classification Name |
bandage, liquid
|
510(k) Number |
K954918 |
Device Name |
COMBIDERM ACD |
Applicant |
CONVATEC, A BRISTOL-MYERS SQUIBB CO. |
P.O. BOX CN 5254 |
PRINCETON,
NJ
08543 -5254
|
|
Applicant Contact |
MCFORD ZAMORE |
Correspondent |
CONVATEC, A BRISTOL-MYERS SQUIBB CO. |
P.O. BOX CN 5254 |
PRINCETON,
NJ
08543 -5254
|
|
Correspondent Contact |
MCFORD ZAMORE |
Regulation Number | 880.5090
|
Classification Product Code |
|
Date Received | 10/26/1995 |
Decision Date | 12/26/1995 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|