PROTECH PLUS— 510(k) K983547

Substantially Equivalent

Protech, Inc.

FDA 510(k) clearance K983547 for PROTECH PLUS, Substantially Equivalent on 1999-01-07. Applicant: Protech, Inc..

Clearance details

Applicant: Protech, Inc.
Product code: Code EBI
Advisory panel: Dental
Date received: 1998-10-09
Decision date: 1999-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

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Adverse events under product code EBI

product code EBI

Other: 1
Total: 1

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.