LITTLE GIANT I & II HANDPIECE CONTROL— 510(k) K801975

Name: FDA 510(k) clearance K801975
Creator: U.S. Food and Drug Administration
Published: 1980-09-09

Substantially Equivalent

Silverman'S

FDA 510(k) clearance K801975 for LITTLE GIANT I & II HANDPIECE CONTROL, Substantially Equivalent on 1980-09-09. Applicant: Silverman'S. Device class: 1.

Clearance details

Applicant: Silverman'S
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1980-08-19
Decision date: 1980-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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