Bunn Model 530 Aspirator

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K870094 ↗

FDA Product Code

BTA

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• I.V. Sentinel

  Class II

  FDA 510(k) K821823 Active Cleared 16 Aug 1982

• Bunn Model #40 Low Pressure Alarm

  Class II

  FDA 510(k) K790370 Active Cleared 28 Mar 1979

• Arizona Oxygen Timer Device

  Class I

  FDA 510(k) K761260 Active Cleared 16 Dec 1976

• Bunn Model 510 Medication Compressor

  Class II

  FDA 510(k) K862628 Active Cleared 7 Aug 1986

• Bunn Lite Oxygen Concentrator

  Class II

  FDA 510(k) K855208 Active Cleared 21 Feb 1986

• John Bunn: Medix Compact Traveller

  Class II

  FDA 510(k) K900854 Active Cleared 23 Apr 1990

See all devices from The John Bunn Co. →