THE MYOLOC SYSTEM— 510(k) K900678

Substantially Equivalent

Winder Research, Inc.

FDA 510(k) clearance K900678 for THE MYOLOC SYSTEM, Substantially Equivalent on 1990-08-13. Applicant: Winder Research, Inc.. Device class: 1.

Clearance details

Applicant: Winder Research, Inc.
Product code: Code EJF
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1990-02-13
Decision date: 1990-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, 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.