Legionella Indirect Fluorescent Antibod

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

510(k) Number

K832896 ↗

FDA Product Code

LHL

Device Class

Class II

Regulation

21 CFR Part 866.3300

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Treatment Table, Model #825-100

  Class II

  FDA 510(k) K930262 Active Cleared 29 Mar 1993

• Traction Table Model #825-200

  Class II

  FDA 510(k) K930259 Active Cleared 24 Mar 1993

• Deluxe C Arm Radiological Table, Model #056-004

  Class II

  FDA 510(k) K921501 Active Cleared 15 May 1992

• Urological C-Arm Table, Model #056-450

  Class II

  FDA 510(k) K922591 Active Cleared 27 Nov 1992

• Cardiac Stress Table, 056-180/Univ Roll Stress Att

  Class II

  FDA 510(k) K926082 Active Cleared 30 Dec 1992

• Thyroid Uptake System & Atomlab 950 Med. Spectrome

  Class I

  FDA 510(k) K932153 Active Cleared 7 Sep 1993

See all devices from Biodan Medical Systems, Ltd. →