510(k) K863658— SALTER LABS 3000 SERIES PERCUSSORS

Substantially Equivalent

Salter Labs

Clearance details

Applicant: Salter Labs
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 1986-09-18
Decision date: 1986-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arvin, CA, 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.