ACRON MC MODIFICATION— 510(k) K991774

Substantially Equivalent

GC America, Inc.

FDA 510(k) clearance K991774 for ACRON MC MODIFICATION, Substantially Equivalent on 1999-07-09. Applicant: GC America, Inc..

Clearance details

Applicant: GC America, Inc.
Product code: Code EBI
Advisory panel: Dental
Date received: 1999-05-25
Decision date: 1999-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alsip, IL, 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.