E-Z FLEX— 510(k) K953456

Substantially Equivalent

Fluid Motion Biotechnologies, Inc.

FDA 510(k) clearance K953456 for E-Z FLEX, Substantially Equivalent on 1996-01-26. Applicant: Fluid Motion Biotechnologies, Inc.. Device class: 1.

Clearance details

Applicant: Fluid Motion Biotechnologies, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1995-07-19
Decision date: 1996-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, 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.