NEOTECH MUCUS TRAP W/CATHETER— 510(k) K890425

Substantially Equivalent

Neotech Products, Inc.

FDA 510(k) clearance K890425 for NEOTECH MUCUS TRAP W/CATHETER, Substantially Equivalent on 1989-04-19. Applicant: Neotech Products, Inc..

Clearance details

Applicant: Neotech Products, Inc.
Product code: Code BSY
Advisory panel: Anesthesiology
Date received: 1989-01-26
Decision date: 1989-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatsworth, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BSY

product code BSY

Death: 3
Injury: 155
Malfunction: 959
Total: 1,117

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.