ENT Forceps

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K822278 ↗

FDA Product Code

GEN

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Nagashima Light Source Unit Sl-5

  Class II

  FDA 510(k) K821709 Active Cleared 25 Jun 1982

• Lancets for Ear Surgery

  Class I

  FDA 510(k) K822279 Active Cleared 25 Aug 1982

• Adenotomes

  Class I

  FDA 510(k) K822262 Active Cleared 25 Aug 1982

• Tonsil Dissectors

  Class I

  FDA 510(k) K822187 Active Cleared 24 Aug 1982

• Mircosurgical Instruments

  Class I

  FDA 510(k) K822195 Active Cleared 25 Aug 1982

• Operative Ear Currettes & Related Item

  Class I

  FDA 510(k) K822006 Active Cleared 12 Aug 1982

See all devices from Kelleher Corp. →