STIMLAB— 510(k) K072200

Substantially Equivalent

Micropace Pty, Ltd.

FDA 510(k) clearance K072200 for STIMLAB, Substantially Equivalent on 2007-10-26. Applicant: Micropace Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Micropace Pty, Ltd.
Product code: Code JOQ
Device class: Class 2
Regulation: 21 CFR 870.1750
Advisory panel: Cardiovascular
Date received: 2007-08-08
Decision date: 2007-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canterbury, Nsw, AU

Download summary PDF View on FDA.gov ↗

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