Daum MRI/Conventional Biopsy Kit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K991366 ↗

FDA Product Code

KNW

Device Class

Class II

Regulation

21 CFR Part 876.1075

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Daum Double-Shoot Bisopsy Gun

  Class II

  FDA 510(k) K010037 Active Cleared 22 Mar 2001

• Daum Neurobiopsy Needle

  Class II

  FDA 510(k) K974631 Active Cleared 9 Mar 1998

• Daum Biopsygun

  Class II

  FDA 510(k) K974576 Active Cleared 6 Mar 1998

• Targogrid

  Class II

  FDA 510(k) K970037 Active Cleared 12 Mar 1997

• Daum Aspirationbiopsy Needle

  Class II

  FDA 510(k) K974575 Active Cleared 6 Mar 1998

• Daum Neurocut Neurobiopsyneedle

  Class II

  FDA 510(k) K990278 Active Cleared 30 Mar 1999

See all devices from Daum Corp. →