ABI VEST AIRWAY CLEARANCE SYSTEM— 510(k) K993629

Substantially Equivalent

American Biosystems, Inc.

FDA 510(k) clearance K993629 for ABI VEST AIRWAY CLEARANCE SYSTEM, Substantially Equivalent on 2000-01-21. Applicant: American Biosystems, Inc..

Clearance details

Applicant: American Biosystems, Inc.
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 1999-10-27
Decision date: 2000-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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.