SUBCLAVIAN CATHETER INSERTION TRAY— 510(k) K802580

Name: FDA 510(k) clearance K802580
Creator: U.S. Food and Drug Administration
Published: 1980-11-12

Substantially Equivalent

American Pharmaseal Div. Ahsc

FDA 510(k) clearance K802580 for SUBCLAVIAN CATHETER INSERTION TRAY, Substantially Equivalent on 1980-11-12. Applicant: American Pharmaseal Div. Ahsc. Device class: 1.

Clearance details

Applicant: American Pharmaseal Div. Ahsc
Product code: Code KXF
Device class: Class 1
Regulation: 21 CFR 880.6025
Advisory panel: General Hospital
Date received: 1980-10-15
Decision date: 1980-11-12
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 KXF

product code KXF

Other: 1
Total: 1

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.