FILTERED VACUUM SAFETY TRAP BOTTLE— 510(k) K855074

Name: FDA 510(k) clearance K855074
Creator: U.S. Food and Drug Administration
Published: 1986-03-13

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K855074 for FILTERED VACUUM SAFETY TRAP BOTTLE, Substantially Equivalent on 1986-03-13. Applicant: Boehringer Laboratories. Device class: 2.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code KDQ
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1985-12-19
Decision date: 1986-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KDQ

product code KDQ

Death: 8
Malfunction: 637
Total: 645

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.