UNIGRAFT— 510(k) K003457

Substantially Equivalent

Unicare Biomedical

FDA 510(k) clearance K003457 for UNIGRAFT, Substantially Equivalent on 2001-01-09. Applicant: Unicare Biomedical. Device class: 2.

Clearance details

Applicant: Unicare Biomedical
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2000-11-07
Decision date: 2001-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

Download summary PDF View on FDA.gov ↗

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