HI-DOW-XP— 510(k) K102598

Substantially Equivalent

Hi-Dow International, Inc.

FDA 510(k) clearance K102598 for HI-DOW-XP, Substantially Equivalent on 2011-05-13. Applicant: Hi-Dow International, Inc..

Clearance details

Applicant: Hi-Dow International, Inc.
Product code: Code NUH
Advisory panel: Neurology
Date received: 2010-09-10
Decision date: 2011-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St Louis, MO, US

Download summary PDF View on FDA.gov ↗

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