510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K212491Substantially Equivalent

Air Relax Pro Model AR-4.0

Diode Art Engineering Doing Business AS Air Relax, Pico Rivera CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K212491 is the FDA 510(k) clearance record for Air Relax Pro Model AR-4.0, a class II device, cleared for Diode Art Engineering Doing Business AS Air Relax on under FDA product code IRP (Massager, Powered Inflatable Tube). FDA records list 2 510(k) clearances for Diode Art Engineering Doing Business AS Air Relax, from to . As of , FDA records show no recalls naming K212491.

Clearance record

Decision date
Received
(24 days to decision)
Product code
IRP Massager, Powered Inflatable Tube
Regulation
21 CFR 890.5650
Device class
Class II
Review panel
Physical Medicine
Applicant
Diode Art Engineering Doing Business AS Air Relax 9535 Brasher St., Pico Rivera CA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code IRP

Trailing 12 months
11 clearances under product code IRP in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code IRP, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20263
May 20262
June 20261
July 20262
August 20261
September 20260
October 20260