VISIOPLAST ACRYLIC RESIN— 510(k) K042414

Substantially Equivalent

Tecres

FDA 510(k) clearance K042414 for VISIOPLAST ACRYLIC RESIN, Substantially Equivalent on 2004-12-29. Applicant: Tecres. Device class: 2.

Clearance details

Applicant: Tecres
Product code: Code GXP
Device class: Class 2
Regulation: 21 CFR 882.5300
Advisory panel: Neurology
Date received: 2004-09-07
Decision date: 2004-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, 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.