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Medical Research Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021168JUMP START, MODEL 970300June 26, 2002
K012766PORTABLE INTENSIVE CARE UNITJanuary 23, 2002
K012030PORTABLE INTENSIVE CARE UNITSeptember 24, 2001
K010207PORTABLE INSTENSIVE CARE UNITJune 14, 2001
K002232AEDEFIBRILLATORDecember 6, 2000
K000712PORTABLE INTENSIVE CARE UNIT, MODEL PICApril 27, 2000
K983307MODIFICATION TO PORTABLE INTENSIVE CARE UNITNovember 20, 1998
K974034PORTABLE INTENSIVE CARE UNITMarch 2, 1998
K952085DPD DEFIBRILLATORJune 5, 1995
K935922360 SLX ADVISORY DEFIBRILLATORDecember 22, 1994
K930548DPD DEFIBRILLATORJune 25, 1993
K884869MODIFIED MRL NEUROPROBE SYSTEM VJune 6, 1989
K885191MRL BLOOD PRESSURE MONITORMay 23, 1989
K880932MRL PACETTE, 450SLLDecember 16, 1988
K882664MRL OXIMETERSeptember 16, 1988
K874204450SLL DEFIBRILLATORJanuary 28, 1988
K840900PORTA PAK 90June 11, 1984
K833751PORTA PULSE III #D320January 11, 1984
K803247TRANSCUTANEOUS ELECT. NERVE STIMULATORMarch 20, 1981