510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Medical Research Laboratories, Inc.

Buffalo Grove, IL, US

Medical Research Laboratories, Inc. appears in FDA device records in Buffalo Grove, IL. FDA records list 19 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
19
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 19 510(k) clearances for Medical Research Laboratories, Inc. between 1981 and 2002. The busiest year on record is 1988, with 3. The most recent is 2002, with 2.

Clearances by year, as a table
510(k) clearance decisions for Medical Research Laboratories, Inc., by decision year
YearClearances
19811
19842
19883
19892
19931
19941
19951
19982
20002
20012
20022
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K021168JUMP START, MODEL 970300MKJSubstantially Equivalent - Subject to Tracking Reg.
K012766PORTABLE INTENSIVE CARE UNITMKJSubstantially Equivalent - Subject to Tracking Reg.
K012030PORTABLE INTENSIVE CARE UNITMKJSubstantially Equivalent
K010207PORTABLE INSTENSIVE CARE UNITMKJSubstantially Equivalent - Subject to Tracking Reg.
K002232AEDEFIBRILLATORMKJSubstantially Equivalent
K000712PORTABLE INTENSIVE CARE UNIT, MODEL PICCCKSubstantially Equivalent
K983307MODIFICATION TO PORTABLE INTENSIVE CARE UNITMKJSubstantially Equivalent
K974034PORTABLE INTENSIVE CARE UNITDROSubstantially Equivalent
K952085DPD DEFIBRILLATORLDDSubstantially Equivalent - Subject to Tracking Reg.
K935922360 SLX ADVISORY DEFIBRILLATORMKJSubstantially Equivalent
K930548DPD DEFIBRILLATORLDDSubstantially Equivalent
K884869MODIFIED MRL NEUROPROBE SYSTEM VGZJSubstantially Equivalent
K885191MRL BLOOD PRESSURE MONITORDXNSubstantially Equivalent
K880932MRL PACETTE, 450SLLDROSubstantially Equivalent
K882664MRL OXIMETERDQASubstantially Equivalent
K874204450SLL DEFIBRILLATORLDDSubstantially Equivalent
K840900PORTA PAK 90LDDSubstantially Equivalent
K833751PORTA PULSE III #D320LDDSubstantially Equivalent
K803247TRANSCUTANEOUS ELECT. NERVE STIMULATORSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain