Device Classification Name |
Gauze/Sponge, Internal
|
510(k) Number |
K760113 |
Device Name |
SPONGE, LAPAROTOMY GAUZE |
Applicant |
PARKE-DAVIS CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
PARKE-DAVIS CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Classification Product Code |
|
Date Received | 06/24/1976 |
Decision Date | 07/15/1976 |
Decision |
Substantially Equivalent
(SESE) |
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|