LOW BACK STRIP (OR) K-BACK— 510(k) K912381

Substantially Equivalent

Katecho, Inc.

FDA 510(k) clearance K912381 for LOW BACK STRIP (OR) K-BACK, Substantially Equivalent on 1992-01-30. Applicant: Katecho, Inc.. Device class: 2.

Clearance details

Applicant: Katecho, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1991-05-29
Decision date: 1992-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Moines, IA, 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.