ULS 8-86— 510(k) K863163

Name: FDA 510(k) clearance K863163
Creator: U.S. Food and Drug Administration
Published: 1986-09-22

Substantially Equivalent

American Instrument Manufacturer'S, Inc.

FDA 510(k) clearance K863163 for ULS 8-86, Substantially Equivalent on 1986-09-22. Applicant: American Instrument Manufacturer'S, Inc.. Device class: 1.

Clearance details

Applicant: American Instrument Manufacturer'S, Inc.
Product code: Code DYN
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1986-08-18
Decision date: 1986-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eureka, MO, US

Download summary PDF View on FDA.gov ↗

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