ORATRONICS ENDOSSEOUS FRAME ASSEMBLY— 510(k) K791366

Name: FDA 510(k) clearance K791366
Creator: U.S. Food and Drug Administration
Published: 1979-10-09

Substantially Equivalent

Oratronics, Inc.

FDA 510(k) clearance K791366 for ORATRONICS ENDOSSEOUS FRAME ASSEMBLY, Substantially Equivalent on 1979-10-09. Applicant: Oratronics, Inc.. Device class: 2.

Clearance details

Applicant: Oratronics, Inc.
Product code: Code NRQ
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1979-07-25
Decision date: 1979-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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