FLEX D-4000— 510(k) K951419

Substantially Equivalent

U.S. Table, Inc.

FDA 510(k) clearance K951419 for FLEX D-4000, Substantially Equivalent on 1995-06-30. Applicant: U.S. Table, Inc.. Device class: 1.

Clearance details

Applicant: U.S. Table, Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1995-03-28
Decision date: 1995-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Allen, VA, 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.