Carotid Artery Clamp & Tools

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K811821 ↗

FDA Product Code

HCE

Device Class

Class II

Regulation

21 CFR Part 882.5175

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Chisel (Osteotome, Gouge, Etc.)

  Class I

  FDA 510(k) K864775 Active Cleared 12 Feb 1987

• Bipolar Micro Coagulator Models 25-1000 & 25-1200

  Class II

  FDA 510(k) K880863 Active Cleared 19 Apr 1988

• Bipolar Coagulating Forceps

  Class II

  FDA 510(k) K811820 Active Cleared 28 Jul 1981

• Bipolar Card

  Class II

  FDA 510(k) K831236 Active Cleared 2 Jun 1983

• Raney and Leroy-Raney Scalp Clip

  Class II

  FDA 510(k) K883963 Active Cleared 7 Oct 1988

• Cranio Blades and Wire Pass Drill

  Class I

  FDA 510(k) K861876 Active Cleared 30 May 1986

See all devices from New England Surgical Instrument Corp. →