510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K822066Substantially Equivalent

Legionella Pneumophila

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

K822066 is the FDA 510(k) clearance record for LEGIONELLA PNEUMOPHILA, 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 K822066.

Clearance record

Decision date
Received
(69 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. P.o.b. 2012, Israel, IL
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