STERILIZING CASE CAT. NO. 65199— 510(k) K800080

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K800080 for STERILIZING CASE CAT. NO. 65199, Substantially Equivalent on 1980-01-28. Applicant: Edward Weck, Inc..

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code FLE
Advisory panel: General Hospital
Date received: 1980-01-14
Decision date: 1980-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FLE

product code FLE

Malfunction: 444
Total: 444

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.