Van Dellen Aspirating Tubing

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K873463 ↗

FDA Product Code

BYY

Device Class

Class II

Regulation

21 CFR Part 880.6740

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Van Dellen Bacteria Filter

  Class II

  FDA 510(k) K873465 Active Cleared 20 Jan 1988

• Van Dellen Retrobulbar Needle

  Class I

  FDA 510(k) K873162 Active Cleared 4 Sep 1987

• Van Dellen Aspirator

  Class II

  FDA 510(k) K873462 Active Cleared 25 Sep 1987

• Van Dellen Irrigating Cystotome

  Class I

  FDA 510(k) K873163 Active Cleared 4 Sep 1987

• Van Dellen Cannula

  Class II

  FDA 510(k) K873464 Active Cleared 23 Nov 1987

• Van Dellen Healon Cannula

  Class I

  FDA 510(k) K873164 Active Cleared 4 Sep 1987