SILIVA EJECTOR/ORAL CAVITY EVACUATOR— 510(k) K864300

Name: FDA 510(k) clearance K864300
Creator: U.S. Food and Drug Administration
Published: 1986-11-24

Substantially Equivalent

Ardent Intl., Inc.

FDA 510(k) clearance K864300 for SILIVA EJECTOR/ORAL CAVITY EVACUATOR, Substantially Equivalent on 1986-11-24. Applicant: Ardent Intl., Inc.. Device class: 1.

Clearance details

Applicant: Ardent Intl., Inc.
Product code: Code DYN
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1986-10-31
Decision date: 1986-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newtown Square, PA, US

Download summary PDF View on FDA.gov ↗

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K924211 — EJECTOR1993-03-31
K920492 — HIGH VAC1992-05-11

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