Kenlor Industries, Inc.
Kenlor Industries, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1997.
Top product codes for Kenlor Industries, Inc.
Recent clearances by Kenlor Industries, Inc.
- K964014 — KENLOR H. PYLORI CONTROL SERUM
- K952840 — KENLOR LIQUID TOTAL URINE CONTROL
- K950326 — KENLOR HUMAN SPINAL FLUID CONTROL
- K903338 — KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL
- K896440 — KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT
- K890618 — COOMASSIE BLUE TOTAL PROTEIN ASSAY KIT
- K890573 — KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT
- K890576 — KENLOR HUMAN SPINAL FLUID CONTROL LIQUID
- K890577 — KENLOR LIQUID URINE CONTROL
Data sourced from openFDA. This site is unofficial and independent of the FDA.