Wako Chemicals USA, Inc.
Wako Chemicals USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2011.
Clearances by Wako Chemicals USA, Inc. — page 2
101–124 of 124- K871765 — PHOSPHOLIPIDS STANDARD SOLUTION CALIBRATOR
- K871766 — TRIGLYCERIDE STANDARD SOLUTION CALIBRATOR
- K871767 — UREA N STANDARD SOLUTION CALIBRATOR
- K871768 — URIC ACID STANDARD SOLUTION CALIBRATOR
- K870401 — WAKO(TM) AUTOKIT LDH
- K864813 — WAKO (TM) AUTOKIT GOT TEST
- K864850 — WAKO(TM) AUTOKIT GPT
- K864303 — QKO (TM) AMYLASE B-HA
- K864302 — WAKO(TM) GOT II - HA
- K864335 — WAKO GPT II - HA
- K861508 — WAKO MICRO TP
- K842847 — WAKO AUTOMATED REAGENTS FOR HITACHI 705
- K842452 — WAKO LDH CII TEST
- K834075 — MAGNESIUM B TEST
- K833257 — WAKO GLUCOSE C
- K832004 — WAKO CPK TEST
- K831639 — WAKO R-GTP C-TEST
- K831687 — WAKO CHOLESTEROL CII
- K830761 — WAKO FREE CHOLESTEROL C TEST
- K830564 — FEB TEST
- K823939 — WAKO INSULIN TEST
- K820241 — WAKO CALCIUM C TEST
- K812081 — WAKO NEFA C TEST
- K811504 — WAKO URIC ACID B TEST
Data sourced from openFDA. This site is unofficial and independent of the FDA.