Device Classification Name |
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
|
510(k) Number |
K830010 |
Device Name |
SUPERJET LANCET |
Applicant |
MEDPROBE LABORATORIES |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
MEDPROBE LABORATORIES |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 878.4850
|
Classification Product Code |
|
Date Received | 01/26/1983 |
Decision Date | 01/26/1983 |
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
|