FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE— 510(k) K841675

Name: FDA 510(k) clearance K841675
Creator: U.S. Food and Drug Administration
Published: 1984-06-27

Substantially Equivalent

Leonard Lorch

FDA 510(k) clearance K841675 for FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE, Substantially Equivalent on 1984-06-27. Applicant: Leonard Lorch. Device class: 1.

Clearance details

Applicant: Leonard Lorch
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1984-04-23
Decision date: 1984-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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