The John Bunn Co.
The John Bunn Co. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1990.
Top product codes for The John Bunn Co.
Recent clearances by The John Bunn Co.
- K900854 — JOHN BUNN: MEDIX COMPACT TRAVELLER
- K883216 — BUNN MODEL 50 OXYGEN FLOW CONTROLLER
- K873071 — BUNN CONCENTRATOR MODEL 2100 SERIES
- K870094 — BUNN MODEL 530 ASPIRATOR
- K861435 — BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVE
- K861199 — BUNN MODEL 22 OXYGEN FLOW CONTROLLER
- K862628 — BUNN MODEL 510 MEDICATION COMPRESSOR
- K855208 — BUNN LITE OXYGEN CONCENTRATOR
- K860060 — RX02 PLUS OXYGEN CONCENTRATOR
- K843811 — BUNN 3001 OXYGEN CONCENTRATOR
- K841102 — BUNN 1000 OXYGEN CONCENTRATOR
- K840534 — LIQUID OXYGEN SYSTEM
- K821823 — I.V. SENTINEL
- K800546 — BUNN VOLUMAIRE RESPIRATORY EXERCISER
- K790370 — BUNN MODEL #40 LOW PRESSURE ALARM
- K780863 — MODEL 65 HIGH & LOW PRESSURE ALARM
- K780862 — MODEL 290 OXYGEN RICH AIR SUPPLY UNIT
- K781213 — COMPRESSOR, AIR, MINI-SILENT
- K761260 — ARIZONA OXYGEN TIMER DEVICE
- K760705 — OXYGEN-RICH
Data sourced from openFDA. This site is unofficial and independent of the FDA.