510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913368Substantially Equivalent

Models Mr700/mr720/mr730 Dual Servo Resp Humid Acc

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

K913368 is the FDA 510(k) clearance record for MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC, a class II device, cleared for Fisher & Paykel Electronics , Ltd. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 17 510(k) clearances for Fisher & Paykel Electronics , Ltd., from to . As of , FDA records show no recalls naming K913368.

Clearance record

Decision date
Received
(173 days to decision)
Product code
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Regulation
21 CFR 868.5450
Device class
Class II
Review panel
Anesthesiology
Applicant
Fisher & Paykel Electronics , Ltd. 25 Carbine Rd. Panmure, Auckland, New Zealand, NZ
510(k) summary
Statement
Third party review
No

Clearances, product code BTT

Trailing 12 months
5 clearances under product code BTT in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BTT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260