EndoVac Pure— 510(k) K162436

Substantially Equivalent

Kerr Corporation

FDA 510(k) clearance K162436 for EndoVac Pure, Substantially Equivalent on 2016-12-21. Applicant: Kerr Corporation. Device class: 1.

Clearance details

Applicant: Kerr Corporation
Product code: Code NYL
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2016-08-31
Decision date: 2016-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CA, 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.