Labsystems, Inc.
Labsystems, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1993.
Top product codes for Labsystems, Inc.
Recent clearances by Labsystems, Inc.
- K923365 — TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM
- K896474 — RESUBMITTED FECATWIN SENSITIVE - FECA-EIA
- K890154 — MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA
- K890091 — MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT
- K881243 — RUBELLA IGG - EIA TEST KIT NUMBER 61 07 201
- K873780 — MODIFICATION RUBELLA IGM EIA TEST KIT
- K873583 — AUTO-EIA
- K872252 — MODIFIED TOXOPLASMA GONDII IGG EIA TEST KIT
- K862705 — CYTOMEGALOVIRUS IGG EIA TEST KIT
- K862431 — RUBELLA IGM EIA TEST KIT
- K862216 — TOXOPLASMA GONDII IGG EIA TEST KIT (AMENDMENT)
- K853696 — RUBELLA IGG EIA TEST KIT
- K843189 — CYTOMEGALOVIRUS IGG EIA TEST KIT
- K842797 — TOXOPLASMA GONDII IGM EIA TEST KIT
- K842773 — LABSYSTEMS FP-901 CHEMISTRY ANALYZER
- K833829 — TOXOPLASMA GOND II IGG DIA TEST KIT
- K841214 — LABSYSTEMS UNISKAN
Data sourced from openFDA. This site is unofficial and independent of the FDA.