EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088— 510(k) K011941

Substantially Equivalent

The Kendall Company

FDA 510(k) clearance K011941 for EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088, Substantially Equivalent on 2001-08-22. Applicant: The Kendall Company.

Clearance details

Applicant: The Kendall Company
Product code: Code FRO
Advisory panel: Unknown
Date received: 2001-06-21
Decision date: 2001-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mansfield, MA, US

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Adverse events under product code FRO

product code FRO

Death: 30
Injury: 653
Malfunction: 479
Other: 11
Total: 1,173

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.