TENSCARE ULTIMA NMS/EMS— 510(k) K023997

Substantially Equivalent

Tenscare, Ltd.

FDA 510(k) clearance K023997 for TENSCARE ULTIMA NMS/EMS, Substantially Equivalent on 2003-03-03. Applicant: Tenscare, Ltd.. Device class: 2.

Clearance details

Applicant: Tenscare, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2002-12-03
Decision date: 2003-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Timperley, Cheshire, GB

Download summary PDF View on FDA.gov ↗

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