BURR, DENTAL— 510(k) K801886

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K801886 for BURR, DENTAL, Substantially Equivalent on 1980-08-20. Applicant: Aesculap Instruments Corp..

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code EJL
Advisory panel: Dental
Date received: 1980-07-28
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code EJL

product code EJL

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.