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Burdick Corp.

Mchenry, IL, US

Burdick Corp. appears in FDA device records in Mchenry, IL. FDA records list 44 510(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
44
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 44 510(k) clearances for Burdick Corp. between 1976 and 1996. The busiest year on record is 1976, with 6. The most recent is 1996, with 3.

Clearances by year, as a table
510(k) clearance decisions for Burdick Corp., by decision year
YearClearances
19766
19774
19784
19792
19804
19811
19821
19842
19852
19861
19873
19893
19901
19912
19943
19952
19963
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K952417QUEST EXERCISE STRESS SYSTEMDSISubstantially Equivalent
K954267BURDICK 200 PULSE OXIMETERDQASubstantially Equivalent
K946281ECLIPSE 4 ELECTROCARDIOGRAPHLOSSubstantially Equivalent
K945985PC HOLTER SCANNING SYSTEM SIMPLICITY, ALTAIR 8200, 8300, 8400DQKSubstantially Equivalent
K943959ECLIPSE 4 ELECTROCARDIOGRAPHLOSSubstantially Equivalent
K942565ALTAIR-DISC RECORDERDQKSubstantially Equivalent
K941351BURDICK PRO2 OXIMETERDQASubstantially Equivalent
K942438ALTAIR 6100 CASSETTE RECORDERDSHSubstantially Equivalent
K904032ELITE II ELECTROCARDIOGRAPHLOSSubstantially Equivalent
K903565E560 ELECTROCARDIOGRAPHLOSSubstantially Equivalent
K900729NEOSERV 824MCJSubstantially Equivalent
K885085ERGOMED 840/ERGOMED 840LDRTSubstantially Equivalent
K892835E350 ELECTROCARDIOGRAPHDPSSubstantially Equivalent
K883440E550 ELECTROCARDIOGRAPHDSISubstantially Equivalent
K873774M300 MONITOR/CONTROLLER T500 TREADMILLDXJSubstantially Equivalent
K870920ELITE ELECTROCARDIOGRAPHLOSSubstantially Equivalent
K870880EK10 ELECTROCARDIOGRAPHDPSSubstantially Equivalent
K852250595 ARRHYTHMIA MONITORING SYSTEMDSISubstantially Equivalent
K842944MONITORING SYSTEM M720DPSSubstantially Equivalent
K844665COMPUTERDXGSubstantially Equivalent
K840440ELECTROCARDIOGRAPH E-340DPSSubstantially Equivalent
K833951E 310 ELECTROCARDIOGRAPHDPSSubstantially Equivalent
K821755TELCOR 2DRTSubstantially Equivalent
K810940THE BETADSISubstantially Equivalent
K801944MULTICHANNEL TELEMETRY SYSTEMDRGSubstantially Equivalent
K801001AMBULATORY MONITOR AM-1DSHSubstantially Equivalent
K792371TELEMETRY SYSTEM XMT-1 & REC-1GYESubstantially Equivalent
K792590AP-1 AUTO PROGRAMMERIOLSubstantially Equivalent
K790292MONITOR, ELECTROCARDIOSCOPEDRTSubstantially Equivalent
K790114ELECTROCARDIOGRAPH, EK-9DPSSubstantially Equivalent
K782059TRANSMITTER, TR-1 ECGDXHSubstantially Equivalent
K780702CSS-60 DIGITAL HEART RATE METERDRTSubstantially Equivalent
K780116AMPLIFIER, PC-700DQCSubstantially Equivalent
K780138EK-670DPSSubstantially Equivalent
K772152CENTRAL MONITORING SYSTEMDXGSubstantially Equivalent
K770240TREADMILL STRESS EXERCISE SYSTEMIOLSubstantially Equivalent
K770239DIGITAL HEART RATE METERDRTSubstantially Equivalent
K760857TR-3 TRANSMITTERDXHSubstantially Equivalent
K760271ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)DPSSubstantially Equivalent
K760272CIRCUIT, PRINTED, SERVO-MECHANISMDPSSubstantially Equivalent
K760268ELECTROCARDIOGRAPH EK-6 W/OPTIONAL CIRC.DPSSubstantially Equivalent
K760266MONITOR, ELECTROCARDIOSCOPEDPSSubstantially Equivalent
K760265ELCTROCARDIOGRAPH, EK-6DPSSubstantially Equivalent
K760275TREADMILL (TMS-300)IOLSubstantially 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