Bougie, Filiform, Jackson

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K770959 ↗

FDA Product Code

KBI

Device Class

Class I

Regulation

21 CFR Part 874.4175

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Telescope, Rigid Endoscope

  Class II

  FDA 510(k) K760177 Active Cleared 30 Aug 1976

• Pfister-Schwartz Stone Retriever

  Class II

  FDA 510(k) K771302 Active Cleared 2 Aug 1977

• Scissor - 1.5mm Probe Point, Angled

  Class I

  FDA 510(k) K760792 Active Cleared 11 Nov 1976

• Teflon Coated Resectoscope Sheath

  Class II

  FDA 510(k) K761242 Active Cleared 16 Dec 1976

• Converse Altar Retractor

  Class I

  FDA 510(k) K760851 Active Cleared 10 Mar 1977

• Sheath, Resectoscope

  Class II

  FDA 510(k) K760182 Active Cleared 2 Dec 1976

See all devices from V. Mueller O.V. Baxter Healthcare Corp. →