PIEZON MASTER 400— 510(k) K896749

Name: FDA 510(k) clearance K896749
Creator: U.S. Food and Drug Administration
Published: 1990-08-31

Substantially Equivalent

Electro Medical Systems (Ems Sa)

FDA 510(k) clearance K896749 for PIEZON MASTER 400, Substantially Equivalent on 1990-08-31. Applicant: Electro Medical Systems (Ems Sa). Device class: 2.

Clearance details

Applicant: Electro Medical Systems (Ems Sa)
Product code: Code ELC
Device class: Class 2
Regulation: 21 CFR 872.4850
Advisory panel: Dental
Date received: 1989-11-30
Decision date: 1990-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nyon, CH

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ELC

product code ELC

Malfunction: 1,255
Total: 1,255

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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