Device Classification Name |
Dermatome
|
510(k) Number |
K861138 |
Device Name |
MASH DERMATOME |
Applicant |
MECRON MEDICAL PRODUCTS, INC. |
938 PORT WASHINGTON BLVD. |
P.O. BOX 1139 |
PORT WASHINGTON,
NY
11050
|
|
Applicant Contact |
EMMANUEL ANAPLIOTIS |
Correspondent |
MECRON MEDICAL PRODUCTS, INC. |
938 PORT WASHINGTON BLVD. |
P.O. BOX 1139 |
PORT WASHINGTON,
NY
11050
|
|
Correspondent Contact |
EMMANUEL ANAPLIOTIS |
Regulation Number | 878.4820
|
Classification Product Code |
|
Date Received | 03/26/1986 |
Decision Date | 04/14/1986 |
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
|
|
|