PERIOGLASS— 510(k) K930115

Substantially Equivalent

Usbiomaterials Corp.

FDA 510(k) clearance K930115 for PERIOGLASS, Substantially Equivalent on 1993-11-04. Applicant: Usbiomaterials Corp.. Device class: 2.

Clearance details

Applicant: Usbiomaterials Corp.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1993-01-11
Decision date: 1993-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alachua, FL, 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.