RITTER STARLIGHT DENTAL OPERATING LIGHT— 510(k) K760707

Name: FDA 510(k) clearance K760707
Creator: U.S. Food and Drug Administration
Published: 1976-10-05

Substantially Equivalent

Ritter Co.

FDA 510(k) clearance K760707 for RITTER STARLIGHT DENTAL OPERATING LIGHT, Substantially Equivalent on 1976-10-05. Applicant: Ritter Co.. Device class: 1.

Clearance details

Applicant: Ritter Co.
Product code: Code EAZ
Device class: Class 1
Regulation: 21 CFR 872.4630
Advisory panel: Dental
Date received: 1976-09-23
Decision date: 1976-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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