TECA MODEL B9 ELECTROMYOGRAPH— 510(k) K781399

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K781399 for TECA MODEL B9 ELECTROMYOGRAPH, Substantially Equivalent on 1978-09-20. 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: 1978-08-15
Decision date: 1978-09-20
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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K894889 — TECA NEUROMAPPER 3861989-12-22

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