REVISED T-SCAN SYSTEM— 510(k) K870032

Substantially Equivalent

Sentek, Inc.

FDA 510(k) clearance K870032 for REVISED T-SCAN SYSTEM, Substantially Equivalent on 1987-02-02. Applicant: Sentek, Inc.. Device class: 1.

Clearance details

Applicant: Sentek, Inc.
Product code: Code EFH
Device class: Class 1
Regulation: 21 CFR 872.6140
Advisory panel: Dental
Date received: 1987-01-05
Decision date: 1987-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.