THE HANDSCAN SYSTEM— 510(k) K893455

Substantially Equivalent

Digital Body Systems, Inc.

FDA 510(k) clearance K893455 for THE HANDSCAN SYSTEM, Substantially Equivalent on 1989-08-30. Applicant: Digital Body Systems, Inc.. Device class: 1.

Clearance details

Applicant: Digital Body Systems, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1989-05-03
Decision date: 1989-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, 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.