510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973161Substantially Equivalent

CPAP Humidifier (Hc 200)

Fisher & Paykel Electronics, Ltd., Auckland, NZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973161 is the FDA 510(k) clearance record for CPAP HUMIDIFIER (HC 200), a class II device, cleared for Fisher & Paykel Electronics , Ltd. on under FDA product code BZD (Ventilator, Non-Continuous (Respirator)). FDA records list 17 510(k) clearances for Fisher & Paykel Electronics , Ltd., from to . As of , FDA records show no recalls naming K973161.

Clearance record

Decision date
Received
(322 days to decision)
Product code
BZD Ventilator, Non-Continuous (Respirator)
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Fisher & Paykel Electronics , Ltd. Healthcare Div., Auckland, NZ
510(k) summary
Summary
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