ESOPHAGEAL TUBE— 510(k) K841349

Name: FDA 510(k) clearance K841349
Creator: U.S. Food and Drug Administration
Published: 1984-07-23

Substantially Equivalent

E. Benson Hood Laboratories, Inc.

FDA 510(k) clearance K841349 for ESOPHAGEAL TUBE, Substantially Equivalent on 1984-07-23. Applicant: E. Benson Hood Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: E. Benson Hood Laboratories, Inc.
Product code: Code KNT
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1984-04-02
Decision date: 1984-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from E. Benson Hood Laboratories, Inc.

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K983878 — CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE1999-01-29
K841350 — SALIVARY BYPASS TUBE1984-07-26
K841266 — MONTGOMERY TRACHEAL T-TUBE1984-06-14
K841347 — LARYNGEAL STENT1984-05-02
K841348 — UMBRELLA KEEL1984-05-02

Adverse events under product code KNT

product code KNT

Death: 192
Injury: 6,034
Malfunction: 4,049
Other: 1
Total: 10,276

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.