510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K170924Substantially Equivalent

AirFit F20

ResMed Corp, Bella Vista, AU / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170924 is the FDA 510(k) clearance record for AirFit F20, a class II device, cleared for Resmed, Ltd. on under FDA product code BZD (Ventilator, Non-Continuous (Respirator)). FDA records list 123 510(k) clearances for Resmed, Ltd., from to . As of , FDA records show 2 recalls naming K170924.

Clearance record

Decision date
Received
(280 days to decision)
Product code
BZD Ventilator, Non-Continuous (Respirator)
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Resmed, Ltd. 1 Elizabeth Macarthur Dr., Bella Vista, AU
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BZD

Trailing 12 months
11 clearances under product code BZD in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BZD, trailing twelve months
MonthClearances
November 20250
December 20252
January 20262
February 20260
March 20260
April 20262
May 20262
June 20261
July 20261
August 20260
September 20261
October 20260