SPINOSCOPE— 510(k) K872836

Substantially Equivalent

Diagnospine Fabrication, Inc.

FDA 510(k) clearance K872836 for SPINOSCOPE, Substantially Equivalent on 1987-09-29. Applicant: Diagnospine Fabrication, Inc.. Device class: 2.

Clearance details

Applicant: Diagnospine Fabrication, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1987-07-17
Decision date: 1987-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada H3h 1e8, CA

Download summary PDF View on FDA.gov ↗

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