Imc Cable/Wire Cover

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K933382 ↗

FDA Product Code

KKX

Device Class

Class II

Regulation

21 CFR Part 878.4370

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Inman Medical Packing Strip

  Class II

  FDA 510(k) K921291 Active Cleared 21 Jan 1993

• Inman Medical Petrolatum Dressing

  Unclassified

  FDA 510(k) K921289 Active Cleared 10 Nov 1992

• Imc Endoscopic Instrument Holder

  Class II

  FDA 510(k) K933371 Active Cleared 6 Aug 1993

• Inman Endoscopic Blunt Dissector

  Class II

  FDA 510(k) K933169 Active Cleared 19 Apr 1994

• 10.0mm Suction/Irrigation Probe & Tubing Kit

  Class II

  FDA 510(k) K932762 Active Cleared 31 Aug 1993

• Imc 5.0mm Irrigation/Aspiration Probe

  Class I

  FDA 510(k) K933305 Active Cleared 5 Oct 1993

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