TECA MODEL-10 ELECTROMYOGRAPH— 510(k) K802637

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K802637 for TECA MODEL-10 ELECTROMYOGRAPH, Substantially Equivalent on 1980-11-26. Applicant: Teca, Inc.. Device class: 2.

Clearance details

Applicant: Teca, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1980-10-22
Decision date: 1980-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Teca, Inc.

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