BREATHING TUBE SUPPORT— 510(k) K933420

Name: FDA 510(k) clearance K933420
Creator: U.S. Food and Drug Administration
Published: 1993-10-13

Substantially Equivalent

Blake Medical, Inc.

FDA 510(k) clearance K933420 for BREATHING TUBE SUPPORT, Substantially Equivalent on 1993-10-13. Applicant: Blake Medical, Inc.. Device class: 1.

Clearance details

Applicant: Blake Medical, Inc.
Product code: Code CBH
Device class: Class 1
Regulation: 21 CFR 868.5770
Advisory panel: Anesthesiology
Date received: 1993-07-13
Decision date: 1993-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tifton, GA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CBH

product code CBH

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.