ULTRASET CATHETER— 510(k) K911294

Name: FDA 510(k) clearance K911294
Creator: U.S. Food and Drug Administration
Published: 1991-06-10

Substantially Equivalent

Dhd Diemolding Healthcare Div.

FDA 510(k) clearance K911294 for ULTRASET CATHETER, Substantially Equivalent on 1991-06-10. Applicant: Dhd Diemolding Healthcare Div.. Device class: 1.

Clearance details

Applicant: Dhd Diemolding Healthcare Div.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1991-03-25
Decision date: 1991-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.