Quick Prime Hemoconcen. No. Hq-7000 and Cbp-7000Q

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K903641 ↗

FDA Product Code

KDI

Device Class

Class II

Regulation

21 CFR Part 876.5860

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Oxygen Saturation Meter Model No. Sm-1

  Not classified

  FDA 510(k) K802847 Active Cleared 16 Dec 1980

• Univox W/Holders, Models Univox-Hl, Hlb, Hlf

  Class II

  FDA 510(k) K894826 Active Cleared 28 Feb 1990

• Q220F Carditomy Reservoir/Modified

  Class II

  FDA 510(k) K790635 Active Cleared 18 Apr 1979

• Flushflo II

  Class II

  FDA 510(k) K812173 Active Cleared 18 Aug 1981

• Bos-2S, Spiraflo Bubble Infant Oxygen.

  Class II

  FDA 510(k) K823273 Active Cleared 5 Jan 1983

• Physiological Pressure Transducer #900

  Class II

  FDA 510(k) K820342 Active Cleared 4 Mar 1982

See all devices from Bentley Laboratories, Inc. →