OXYFRESH OXYCARE 3000— 510(k) K910832

Substantially Equivalent

Oxyfresh

FDA 510(k) clearance K910832 for OXYFRESH OXYCARE 3000, Substantially Equivalent on 1991-04-17. Applicant: Oxyfresh. Device class: 1.

Clearance details

Applicant: Oxyfresh
Product code: Code EFS
Device class: Class 1
Regulation: 21 CFR 872.6510
Advisory panel: Dental
Date received: 1991-02-27
Decision date: 1991-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spokane, WA, US

Download summary PDF View on FDA.gov ↗

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K952234 — BARRIER ALL FILM1995-07-31

Data sourced from openFDA. This site is unofficial and independent of the FDA.