Device Classification Name |
electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed
|
510(k) Number |
K120040 |
Device Name |
REPROCESSED SURGICAL ELECTRIC INSTRUMENT |
Applicant |
STERILMED, INC. |
11400 73rd Ave N Ste 100 |
MAPLE GROVE,
MN
55369
|
|
Applicant Contact |
JASON SKRAMSTED |
Correspondent |
STERILMED, INC. |
11400 73rd Ave N Ste 100 |
MAPLE GROVE,
MN
55369
|
|
Correspondent Contact |
JASON SKRAMSTED |
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 01/05/2012 |
Decision Date | 10/05/2012 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|