RESPIRATORY HUMIDIFIER, MODEL # MR850— 510(k) K983112

Substantially Equivalent

Fisher & Paykel Healthcare, Ltd.

FDA 510(k) clearance K983112 for RESPIRATORY HUMIDIFIER, MODEL # MR850, Substantially Equivalent on 1998-11-10. Applicant: Fisher & Paykel Healthcare, Ltd..

Clearance details

Applicant: Fisher & Paykel Healthcare, Ltd.
Product code: Code BTT
Advisory panel: Anesthesiology
Date received: 1998-09-04
Decision date: 1998-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Auckland, 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.