King Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 41 products
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Total Devices41
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K933329 | KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT | JMO | 1993-10-22 | View |
| 510(k) | K931834 | KING SODIUM/POTASSIUM STANDARD MODIFIED | JIS | 1993-08-25 | View |
| 510(k) | K931773 | HDL PRECIPITATING REAGENT (DEXTRAN SULFATE) | LBR | 1993-08-16 | View |
| 510(k) | K931326 | KING DIAGNOSTICS CK REAGENT | CGS | 1993-06-15 | View |
| 510(k) | K923129 | KING DIAGNOSTICS GLUCOSE (HK) REAGENT | CFR | 1992-11-02 | View |
| 510(k) | K922969 | KING DIAGNOSTICS UREA NITROGEN REAGENT | CDN | 1992-10-13 | View |
| 510(k) | K922921 | KING DIAGNOSTICS CHLORIDE REAGENT | CHJ | 1992-10-05 | View |
| 510(k) | K923927 | KING DIAGNOSTICS MAGNESIUM REAGENT | JGJ | 1992-09-30 | View |
| 510(k) | K923091 | KING DIAGNOSTICS GAMMA GT REAGENT | JPZ | 1992-09-09 | View |
| 510(k) | K923128 | KING DIAGNOSTICS CHOLESTEROL REAGENT | CHH | 1992-09-09 | View |
| 510(k) | K922964 | KING DIAGNOSTIC TRIGLYCERIDES REAGENT | CDT | 1992-08-18 | View |
| 510(k) | K922835 | CALCIUM (AZ III) REAGENT | CJY | 1992-08-04 | View |
| 510(k) | K922108 | KING DIAGNOSTICS AST (GOT) REAGENT | CIT | 1992-07-15 | View |
| 510(k) | K922109 | KING DIAGNOSTICS ALT (GPT) REAGENT | CKA | 1992-06-04 | View |
| 510(k) | K920809 | KING DIAGNOSTICS SODIUM/POTASSIUM STANDARD | JIS | 1992-04-17 | View |
| 510(k) | K912499 | KING DIAGNOSTICS CHOLESTEROL REAGENT STRIP TEST | CHH | 1991-09-27 | View |
| 510(k) | K912251 | KING DIAGNOSTICS GLUCOSE (HK) REAGENT STRIP TEST | CFR | 1991-07-18 | View |
| 510(k) | K884485 | KD ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT | GFO | 1988-12-28 | View |
| 510(k) | K883640 | KD ONE-STAGE PROTHROMBIN TIME TEST | JPA | 1988-10-31 | View |
| 510(k) | K883637 | KD 0.02 M CALCIUM CHLORIDE SOLUTION | JPA | 1988-10-31 | View |
No matching devices.
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