Kenlor Industries, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K964014 | KENLOR H. PYLORI CONTROL SERUM | LYR | 1997-03-03 | View |
| 510(k) | K952840 | KENLOR LIQUID TOTAL URINE CONTROL | JJW | 1995-07-19 | View |
| 510(k) | K950326 | KENLOR HUMAN SPINAL FLUID CONTROL | JJY | 1995-03-20 | View |
| 510(k) | K903338 | KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL | JJY | 1990-09-07 | View |
| 510(k) | K896440 | KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT | JIR | 1990-02-16 | View |
| 510(k) | K890618 | COOMASSIE BLUE TOTAL PROTEIN ASSAY KIT | CEK | 1989-05-22 | View |
| 510(k) | K890573 | KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT | JIY | 1989-03-24 | View |
| 510(k) | K890576 | KENLOR HUMAN SPINAL FLUID CONTROL LIQUID | JJY | 1989-03-09 | View |
| 510(k) | K890577 | KENLOR LIQUID URINE CONTROL | JJW | 1989-03-09 | View |
No matching devices.
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