AMPLAID EMG15— 510(k) K884071

Substantially Equivalent

Amplus Corp.

FDA 510(k) clearance K884071 for AMPLAID EMG15, Substantially Equivalent on 1989-02-27. Applicant: Amplus Corp.. Device class: 2.

Clearance details

Applicant: Amplus Corp.
Product code: Code GWL
Device class: Class 2
Regulation: 21 CFR 882.1835
Advisory panel: Neurology
Date received: 1988-09-27
Decision date: 1989-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

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More clearances from Amplus Corp.

K903066 — AMPLAID 770 ADMITTANCE METER1990-10-24
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Data sourced from openFDA. This site is unofficial and independent of the FDA.