EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.— 510(k) K800456

Substantially Equivalent

Khi, Inc.

FDA 510(k) clearance K800456 for EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR., Substantially Equivalent on 1980-03-18. Applicant: Khi, Inc..

Clearance details

Applicant: Khi, Inc.
Product code: Code BTL
Advisory panel: Anesthesiology
Date received: 1980-02-29
Decision date: 1980-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code BTL

product code BTL

Death: 8
Malfunction: 3,256
Other: 1
Total: 3,265

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.