510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832896Substantially Equivalent

Legionella Indirect Fluorescent Antibod

Biodan Medical Systems, Ltd., Rehovot, Israel / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832896 is the FDA 510(k) clearance record for LEGIONELLA INDIRECT FLUORESCENT ANTIBOD, a class II device, cleared for Biodan Medical Systems, Ltd. on under FDA product code LHL (Reagents, Antibody, Legionella, Direct & Indirect Fluorescent). FDA records list 20 510(k) clearances for Biodan Medical Systems, Ltd., from to . As of , FDA records show no recalls naming K832896.

Clearance record

Decision date
Received
(52 days to decision)
Product code
LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
Regulation
21 CFR 866.3300
Device class
Class II
Review panel
Microbiology
Applicant
Biodan Medical Systems, Ltd. Kiryat Weizmann, Rehovot, Israel
Third party review
No

Clearances, product code LHL

Trailing 12 months

FDA records hold no clearances under product code LHL in the trailing twelve months.

FDA records show no clearances under product code LHL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LHL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260