Device Classification Name |
Cap, Cervical
|
510(k) Number |
K900162 |
Device Name |
DGH A-SAN PROBE HOLDER |
Applicant |
JEDMED INSTRUMENT CO. |
1430 HANLEY INDUSTRIAL CT. |
ST. LOUIS,
MO
63144
|
|
Applicant Contact |
CRAIG RAPP |
Correspondent |
JEDMED INSTRUMENT CO. |
1430 HANLEY INDUSTRIAL CT. |
ST. LOUIS,
MO
63144
|
|
Correspondent Contact |
CRAIG RAPP |
Regulation Number | 884.5250
|
Classification Product Code |
|
Date Received | 01/12/1990 |
Decision Date | 02/16/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|