DESERET EPIDURAL CATHETER— 510(k) K850439

Name: FDA 510(k) clearance K850439
Creator: U.S. Food and Drug Administration
Published: 1985-03-05

Substantially Equivalent

Parke-Davis Co.

FDA 510(k) clearance K850439 for DESERET EPIDURAL CATHETER, Substantially Equivalent on 1985-03-05. Applicant: Parke-Davis Co.. Device class: 2.

Clearance details

Applicant: Parke-Davis Co.
Product code: Code BSO
Device class: Class 2
Regulation: 21 CFR 868.5120
Advisory panel: Anesthesiology
Date received: 1985-02-05
Decision date: 1985-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, MI, US

Download summary PDF View on FDA.gov ↗

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K855120 — ATI DISPOSABLE BIOLOGICAL TEST PACK1986-06-18
K860570 — ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE1986-03-31
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Adverse events under product code BSO

product code BSO

Malfunction: 688
Total: 688

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.