MODIFICATION TO A620 EEG— 510(k) K012011

Substantially Equivalent

Stoelting Co.

FDA 510(k) clearance K012011 for MODIFICATION TO A620 EEG, Substantially Equivalent on 2001-10-10. Applicant: Stoelting Co.. Device class: 2.

Clearance details

Applicant: Stoelting Co.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 2001-06-28
Decision date: 2001-10-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Wood Dale, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Stoelting Co.

K965006 — AT 62 EEG (A.K.A THE A; PHA-THETA TRAINER)1997-02-05
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Data sourced from openFDA. This site is unofficial and independent of the FDA.