Medical Research Laboratories, Inc.
FDA 510(k) medical device clearances.
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.