POWERED PATIENT SYSTEM— 510(k) K810220

Substantially Equivalent

Tri W-G, Inc.

FDA 510(k) clearance K810220 for POWERED PATIENT SYSTEM, Substantially Equivalent on 1981-02-04. Applicant: Tri W-G, Inc.. Device class: 2.

Clearance details

Applicant: Tri W-G, Inc.
Product code: Code IKZ
Device class: Class 2
Regulation: 21 CFR 890.5225
Advisory panel: Physical Medicine
Date received: 1981-01-27
Decision date: 1981-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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