Endoscopic Aspiration Catheter Set

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844691 ↗

FDA Product Code

OCX

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Endoscopic Multiple Biopsy Instrument

  Class I

  FDA 510(k) K844690 Active Cleared 2 Jan 1985

• Fecal Staining Kit

  Class I

  FDA 510(k) K810875 Active Cleared 1 May 1981

• Foreign Body Protector

  Class II

  FDA 510(k) K841258 Active Cleared 9 Jul 1984

• Liver Biopsy Tray

  Not classified

  FDA 510(k) K842001 Active Cleared 15 Oct 1984

• Endo-Guard

  Class I

  FDA 510(k) K830781 Active Cleared 31 Mar 1983

• Endoscopic Manual Air Insufflator

  Class II

  FDA 510(k) K844689 Active Cleared 2 Jan 1985

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