GENERAL ELECTRIC PANELIPSE LD— 510(k) K792581

Name: FDA 510(k) clearance K792581
Creator: U.S. Food and Drug Administration
Published: 1980-01-16

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K792581 for GENERAL ELECTRIC PANELIPSE LD, Substantially Equivalent on 1980-01-16. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1979-12-14
Decision date: 1980-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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