K982889

Substantially Equivalent

MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000

Applicant: Electromed, Inc.
Product code: BYI
Advisory panel: Anesthesiology
Date received: 1998-08-17
Decision date: 1999-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Adverse events under product code BYI

product code BYI

Death: 3
Total: 3

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.