3D DENTAL DIAMOND ROTARY INSTRUMENTS— 510(k) K893844

Name: FDA 510(k) clearance K893844
Creator: U.S. Food and Drug Administration
Published: 1989-08-11

Substantially Equivalent

Lustgarten Multi-Tech International, Inc.

FDA 510(k) clearance K893844 for 3D DENTAL DIAMOND ROTARY INSTRUMENTS, Substantially Equivalent on 1989-08-11. Applicant: Lustgarten Multi-Tech International, Inc.. Device class: 1.

Clearance details

Applicant: Lustgarten Multi-Tech International, Inc.
Product code: Code DZP
Device class: Class 1
Regulation: 21 CFR 872.4535
Advisory panel: Dental
Date received: 1989-05-25
Decision date: 1989-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Framingham, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.