Instrumentation Laboratory CO
Instrumentation Laboratory CO holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2023, with 31 FDA device recalls on record.
Clearances by Instrumentation Laboratory CO — page 4
301–321 of 321- K771472 — MULTISTAT III TRIGLYCERIDE TEST
- K770994 — FURNACE AUTOSAMPLER, MODEL 155
- K771441 — MULTISTAT III CPK TEST
- K771442 — MULTISTAT III UREA NITROGEN TEST
- K771443 — MULTISTAT III CREATININE TEST
- K770946 — RECORD, MODEL 702, I.L.
- K770228 — AQUEOUS PH/BLOOD GAS CONTROLS
- K770645 — SPECTROPHOTOMETER, MODEL 751
- K770660 — ANALYZER, CENTRIFUGAL, IL MULTISTAT III
- K760969 — PH/BLOOD GAS SYSTEM
- K760975 — WEIL ONCOMETER (IL 186)
- K760448 — SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT
- K760211 — ANALYZER, GLUCOSE/UREA/CREATININE
- K760232 — PRINTER, IL 460
- K760233 — TABLE, SAMPLE IL 461
- K760208 — OXIMETER, CO-, IL MODEL 282
- K760064 — CATHETER, THERMAL DILUTION, ANIMAL & PED
- K760065 — CATHETER, THERMAL DILUTION, PEDIATRIC
- K760066 — TRAY, ICED INJECTABLE (26420)
- K760067 — CATHETER, THERMAL DILUTION, OPEN CHEST
- K760119 — SAMPLER, FLAMELESS (IL MODEL 555)
Data sourced from openFDA. This site is unofficial and independent of the FDA.