510(k) K895670— SURGICAL SUCTION APPARATUS

Substantially Equivalent

Baker-Sundt Research, Inc.

Clearance details

Applicant: Baker-Sundt Research, Inc.
Product code: Code GEA
Advisory panel: General, Plastic Surgery
Date received: 1989-09-19
Decision date: 1989-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Adverse events under product code GEA

product code GEA

Malfunction: 587
Total: 587

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.