Device Classification Name |
Phosphomolybdate (Colorimetric), Inorganic Phosphorus
|
510(k) Number |
K811749 |
Device Name |
KING DIAGNOSTICS PHOSPHORUS TEST |
Applicant |
KING DIAGNOSTICS, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
KING DIAGNOSTICS, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 862.1580
|
Classification Product Code |
|
Date Received | 06/22/1981 |
Decision Date | 07/10/1981 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|