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The John Bunn Co.

Mchenry, IL, US

The John Bunn Co. appears in FDA device records in Mchenry, IL. FDA records list 20 510(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
20
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 20 510(k) clearances for The John Bunn Co. between 1976 and 1990. The busiest year on record is 1986, with 5. The most recent is 1990, with 1.

Clearances by year, as a table
510(k) clearance decisions for The John Bunn Co., by decision year
YearClearances
19762
19783
19791
19801
19821
19843
19865
19872
19881
19901
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K900854JOHN BUNN: MEDIX COMPACT TRAVELLERBTTSubstantially Equivalent
K883216BUNN MODEL 50 OXYGEN FLOW CONTROLLERNFBSubstantially Equivalent
K873071BUNN CONCENTRATOR MODEL 2100 SERIESCAWSubstantially Equivalent
K870094BUNN MODEL 530 ASPIRATORBTASubstantially Equivalent
K861435BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVECAWSubstantially Equivalent
K861199BUNN MODEL 22 OXYGEN FLOW CONTROLLERNFBSubstantially Equivalent
K862628BUNN MODEL 510 MEDICATION COMPRESSORBTISubstantially Equivalent
K855208BUNN LITE OXYGEN CONCENTRATORCAWSubstantially Equivalent
K860060RX02 PLUS OXYGEN CONCENTRATORCAWSubstantially Equivalent
K843811BUNN 3001 OXYGEN CONCENTRATORCAWSubstantially Equivalent
K841102BUNN 1000 OXYGEN CONCENTRATORCAWSubstantially Equivalent
K840534LIQUID OXYGEN SYSTEMBYJSubstantially Equivalent
K821823I.V. SENTINELFLNSubstantially Equivalent
K800546BUNN VOLUMAIRE RESPIRATORY EXERCISERBWFSubstantially Equivalent
K790370BUNN MODEL #40 LOW PRESSURE ALARMCAPSubstantially Equivalent
K780863MODEL 65 HIGH & LOW PRESSURE ALARMCAPSubstantially Equivalent
K780862MODEL 290 OXYGEN RICH AIR SUPPLY UNITCAWSubstantially Equivalent
K781213COMPRESSOR, AIR, MINI-SILENTBTISubstantially Equivalent
K761260ARIZONA OXYGEN TIMER DEVICEBXPSubstantially Equivalent
K760705OXYGEN-RICHCAWSubstantially 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