LED STIMULATOR LS-05— 510(k) K834442

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K834442 for LED STIMULATOR LS-05, Substantially Equivalent on 1984-08-08. Applicant: Teca, Inc.. Device class: 2.

Clearance details

Applicant: Teca, Inc.
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 1983-12-16
Decision date: 1984-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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