ACUPLUS— 510(k) K954334

Substantially Equivalent

S.H.P. Intl. Pty., Ltd.

FDA 510(k) clearance K954334 for ACUPLUS, Substantially Equivalent on 1996-01-22. Applicant: S.H.P. Intl. Pty., Ltd.. Device class: 2.

Clearance details

Applicant: S.H.P. Intl. Pty., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1995-09-18
Decision date: 1996-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eugene, OR, 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.