NYHUS/NELSON TUBE— 510(k) K851672

Name: FDA 510(k) clearance K851672
Creator: U.S. Food and Drug Administration
Published: 1985-07-09

Substantially Equivalent

Bissell Medical Products, Inc.

FDA 510(k) clearance K851672 for NYHUS/NELSON TUBE, Substantially Equivalent on 1985-07-09. Applicant: Bissell Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Bissell Medical Products, Inc.
Product code: Code KNT
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1985-04-23
Decision date: 1985-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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K873441 — BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE1987-10-27
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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.