510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K933454Substantially Equivalent

Dynamic Germicidal Air Purification System

L&H Airco, Rocklin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933454 is the FDA 510(k) clearance record for DYNAMIC GERMICIDAL AIR PURIFICATION SYSTEM, a class II device, cleared for L&H Airco on under FDA product code FRA (Purifier, Air, Ultraviolet, Medical). FDA records list one 510(k) clearance for L&H Airco. As of , FDA records show no recalls naming K933454.

Clearance record

Decision date
Received
(429 days to decision)
Product code
FRA Purifier, Air, Ultraviolet, Medical
Regulation
21 CFR 880.6500
Device class
Class II
Review panel
General Hospital
Applicant
L&H Airco 3835 Atherton Rd., Suite 7, Rocklin CA
510(k) summary
Statement
Third party review
No

Clearances, product code FRA

Trailing 12 months

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

FDA records show no clearances under product code FRA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FRA, 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