PACIFIC IMPLANT TITANIUM ENDODONTIC POINT— 510(k) K992582

Name: FDA 510(k) clearance K992582
Creator: U.S. Food and Drug Administration
Published: 1999-10-21

Substantially Equivalent

Pacific Implant, Inc.

FDA 510(k) clearance K992582 for PACIFIC IMPLANT TITANIUM ENDODONTIC POINT, Substantially Equivalent on 1999-10-21. Applicant: Pacific Implant, Inc.. Device class: 1.

Clearance details

Applicant: Pacific Implant, Inc.
Product code: Code EKL
Device class: Class 1
Regulation: 21 CFR 872.3840
Advisory panel: Dental
Date received: 1999-08-02
Decision date: 1999-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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