FLO-BOOT— 510(k) K003272

Substantially Equivalent

Discovery Group, LLC

FDA 510(k) clearance K003272 for FLO-BOOT, Substantially Equivalent on 2001-04-04. Applicant: Discovery Group, LLC. Device class: 1.

Clearance details

Applicant: Discovery Group, LLC
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 2000-10-18
Decision date: 2001-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, 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.