BREATHING FILTER— 510(k) K931217

Name: FDA 510(k) clearance K931217
Creator: U.S. Food and Drug Administration
Published: 1993-04-23

Substantially Equivalent

Teknor Medical Products, Inc.

FDA 510(k) clearance K931217 for BREATHING FILTER, Substantially Equivalent on 1993-04-23. Applicant: Teknor Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Teknor Medical Products, Inc.
Product code: Code CAH
Device class: Class 2
Regulation: 21 CFR 868.5260
Advisory panel: Anesthesiology
Date received: 1993-03-10
Decision date: 1993-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Trenton, Ontario, CA

Download summary PDF View on FDA.gov ↗

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K931216 — CONNECTORS AND AIRWAY EXTENSIONS1993-04-23

Adverse events under product code CAH

product code CAH

Death: 7
Total: 7

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.