CATHETER, UMBILICAL ARTERY— 510(k) K760966

Name: FDA 510(k) clearance K760966
Creator: U.S. Food and Drug Administration
Published: 1977-01-26

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760966 for CATHETER, UMBILICAL ARTERY, Substantially Equivalent on 1977-01-26. Applicant: Sherwood Medical Industries. Device class: 2.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code FOS
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 1976-11-04
Decision date: 1977-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FOS

product code FOS

Death: 12
Other: 1
Total: 13

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.