JOY LIGHT— 510(k) K771249

Substantially Equivalent

M.D. Intl., Inc.

FDA 510(k) clearance K771249 for JOY LIGHT, Substantially Equivalent on 1977-07-15. Applicant: M.D. Intl., Inc.. Device class: 1.

Clearance details

Applicant: M.D. Intl., Inc.
Product code: Code EAZ
Device class: Class 1
Regulation: 21 CFR 872.4630
Advisory panel: Dental
Date received: 1977-07-07
Decision date: 1977-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, 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.