Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K211194Substantially Equivalent

Molekule Air Pro

Molekule, Inc., San Francisco CA / Traditional, Substantially Equivalent

K211194 is the FDA 510(k) clearance record for Molekule Air Pro, a class II device, cleared for Molekule, Inc. on under FDA product code FRA (Purifier, Air, Ultraviolet, Medical). FDA records list 3 510(k) clearances for Molekule, Inc., from to . As of , FDA records show no recalls naming K211194.

Clearance record

Decision date
Received
(121 days to decision)
Product code
FRA Purifier, Air, Ultraviolet, Medical
Regulation
21 CFR 880.6500
Device class
Class II
Review panel
General Hospital
Applicant
Molekule, Inc. 1301 Folsom St., San Francisco CA
510(k) summary
Summary PDF
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