Medical Research Laboratories, Inc.
Medical Research Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2002.
Top product codes for Medical Research Laboratories, Inc.
Recent clearances by Medical Research Laboratories, Inc.
- K021168 — JUMP START, MODEL 970300
- K012766 — PORTABLE INTENSIVE CARE UNIT
- K012030 — PORTABLE INTENSIVE CARE UNIT
- K010207 — PORTABLE INSTENSIVE CARE UNIT
- K002232 — AEDEFIBRILLATOR
- K000712 — PORTABLE INTENSIVE CARE UNIT, MODEL PIC
- K983307 — MODIFICATION TO PORTABLE INTENSIVE CARE UNIT
- K974034 — PORTABLE INTENSIVE CARE UNIT
- K952085 — DPD DEFIBRILLATOR
- K935922 — 360 SLX ADVISORY DEFIBRILLATOR
- K930548 — DPD DEFIBRILLATOR
- K884869 — MODIFIED MRL NEUROPROBE SYSTEM V
- K885191 — MRL BLOOD PRESSURE MONITOR
- K880932 — MRL PACETTE, 450SLL
- K882664 — MRL OXIMETER
- K874204 — 450SLL DEFIBRILLATOR
- K840900 — PORTA PAK 90
- K833751 — PORTA PULSE III #D320
- K803247 — TRANSCUTANEOUS ELECT. NERVE STIMULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.