The Slide— 510(k) K203712

Substantially Equivalent

Biotex, Inc.

FDA 510(k) clearance K203712 for The Slide, Substantially Equivalent on 2021-07-20. Applicant: Biotex, Inc.. Device class: 2.

Clearance details

Applicant: Biotex, Inc.
Product code: Code LQZ
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 2020-12-21
Decision date: 2021-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.