MODELS MR410 & MR480 RESPIRATORY HUMIDIFIER/ACCESS— 510(k) K913367

Substantially Equivalent

Fisher & Paykel Electronics , Ltd.

FDA 510(k) clearance K913367 for MODELS MR410 & MR480 RESPIRATORY HUMIDIFIER/ACCESS, Substantially Equivalent on 1992-06-25. Applicant: Fisher & Paykel Electronics , Ltd..

Clearance details

Applicant: Fisher & Paykel Electronics , Ltd.
Product code: Code BTT
Advisory panel: Anesthesiology
Date received: 1991-07-24
Decision date: 1992-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Auckland, New Zealand, NZ

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Adverse events under product code BTT

product code BTT

Death: 60
Injury: 152
Malfunction: 7,232
Other: 2
Total: 7,446

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.