BIODEX SYSTEM 2 AUTOPROGRAM— 510(k) K915648

Substantially Equivalent

Biodex Corp.

FDA 510(k) clearance K915648 for BIODEX SYSTEM 2 AUTOPROGRAM, Substantially Equivalent on 1992-01-09. 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: 1991-12-13
Decision date: 1992-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, US

Download summary PDF View on FDA.gov ↗

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More clearances from Biodex Corp.

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K900741 — BIODEX BACK SYSTEM ATTACHMENT1990-02-26

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