Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Medical Research Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 19 products

Total Devices19
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K021168 JUMP START, MODEL 970300MKJ2002-06-26 View
510(k) K012766 PORTABLE INTENSIVE CARE UNITMKJ2002-01-23 View
510(k) K012030 PORTABLE INTENSIVE CARE UNITMKJ2001-09-24 View
510(k) K010207 PORTABLE INSTENSIVE CARE UNITMKJ2001-06-14 View
510(k) K002232 AEDEFIBRILLATORMKJ2000-12-06 View
510(k) K000712 PORTABLE INTENSIVE CARE UNIT, MODEL PICCCK2000-04-27 View
510(k) K983307 MODIFICATION TO PORTABLE INTENSIVE CARE UNITMKJ1998-11-20 View
510(k) K974034 PORTABLE INTENSIVE CARE UNITDRO1998-03-02 View
510(k) K952085 DPD DEFIBRILLATORLDD1995-06-05 View
510(k) K935922 360 SLX ADVISORY DEFIBRILLATORMKJ1994-12-22 View
510(k) K930548 DPD DEFIBRILLATORLDD1993-06-25 View
510(k) K884869 MODIFIED MRL NEUROPROBE SYSTEM VGZJ1989-06-06 View
510(k) K885191 MRL BLOOD PRESSURE MONITORDXN1989-05-23 View
510(k) K880932 MRL PACETTE, 450SLLDRO1988-12-16 View
510(k) K882664 MRL OXIMETERDQA1988-09-16 View
510(k) K874204 450SLL DEFIBRILLATORLDD1988-01-28 View
510(k) K840900 PORTA PAK 90LDD1984-06-11 View
510(k) K833751 PORTA PULSE III #D320LDD1984-01-11 View
510(k) K803247 TRANSCUTANEOUS ELECT. NERVE STIMULATOR1981-03-20 View
↑