DENTOLOCK— 510(k) K921071

Substantially Equivalent

Dentmed , Ltd.

FDA 510(k) clearance K921071 for DENTOLOCK, Substantially Equivalent on 1992-03-26. Applicant: Dentmed , Ltd.. Device class: 2.

Clearance details

Applicant: Dentmed , Ltd.
Product code: Code KOB
Device class: Class 2
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1992-03-06
Decision date: 1992-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.