510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K002839Substantially Equivalent

End Expiratory Filter, Model Rt020

Fisher & Paykel Healthcare, Inc., East Tamaki, Auckland, NZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002839 is the FDA 510(k) clearance record for END EXPIRATORY FILTER, MODEL RT020, a class II device, cleared for Fisher & Paykel Healthcare, Ltd. on under FDA product code CAH (Filter, Bacterial, Breathing-Circuit). FDA records list 86 510(k) clearances for Fisher & Paykel Healthcare, Ltd., from to . As of , FDA records show no recalls naming K002839.

Clearance record

Decision date
Received
(387 days to decision)
Product code
CAH Filter, Bacterial, Breathing-Circuit
Regulation
21 CFR 868.5260
Device class
Class II
Review panel
Anesthesiology
Applicant
Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Pl., East Tamaki, Auckland, NZ
510(k) summary
Summary
Third party review
No

Clearances, product code CAH

Trailing 12 months
2 clearances under product code CAH in the twelve months to November 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAH, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260