LIQUIBAND DENTAL— 510(k) K993556

Substantially Equivalent

Medlogic Global Corp.

FDA 510(k) clearance K993556 for LIQUIBAND DENTAL, Substantially Equivalent on 2000-01-03. Applicant: Medlogic Global Corp.. Device class: 2.

Clearance details

Applicant: Medlogic Global Corp.
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1999-10-20
Decision date: 2000-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colorado Springs, CO, US

Download summary PDF View on FDA.gov ↗

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