HH SUBCUTANEOUS ACCESS PORT— 510(k) K833672

Name: FDA 510(k) clearance K833672
Creator: U.S. Food and Drug Administration
Published: 1984-03-06

Substantially Equivalent

Holter-Hausner Intl.

FDA 510(k) clearance K833672 for HH SUBCUTANEOUS ACCESS PORT, Substantially Equivalent on 1984-03-06. Applicant: Holter-Hausner Intl.. Device class: 2.

Clearance details

Applicant: Holter-Hausner Intl.
Product code: Code LKG
Device class: Class 2
Regulation: 21 CFR 882.5550
Advisory panel: Neurology
Date received: 1983-10-18
Decision date: 1984-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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