Device Classification Name |
Orthosis, Truncal, For Dysmenorrhea
|
510(k) Number |
K003128 |
Device Name |
MODIFICATION TO RELIEF BRIEF |
Applicant |
THE JM KOHN CO. |
201 SPEAR ST. |
SUITE 1600 |
SAN FRANCISCO,
CA
94105 -1635
|
|
Applicant Contact |
CHARLES L MORIN |
Correspondent |
THE JM KOHN CO. |
201 SPEAR ST. |
SUITE 1600 |
SAN FRANCISCO,
CA
94105 -1635
|
|
Correspondent Contact |
CHARLES L MORIN |
Regulation Number | 890.3490
|
Classification Product Code |
|
Date Received | 10/06/2000 |
Decision Date | 08/12/2002 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Physical Medicine
|
510k Review Panel |
Physical Medicine
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|