BIODEX BACK SYSTEM ATTACHMENT— 510(k) K900741

Substantially Equivalent

Biodex Corp.

FDA 510(k) clearance K900741 for BIODEX BACK SYSTEM ATTACHMENT, Substantially Equivalent on 1990-02-26. Applicant: Biodex Corp.. Device class: 2.

Clearance details

Applicant: Biodex Corp.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1990-02-16
Decision date: 1990-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, 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.