ANTIMICROBIAL REMOVAL DEVICE— 510(k) K810613

Substantially Equivalent

Marion Laboratories, Inc.

FDA 510(k) clearance K810613 for ANTIMICROBIAL REMOVAL DEVICE, Substantially Equivalent on 1981-04-03. Applicant: Marion Laboratories, Inc..

Clearance details

Applicant: Marion Laboratories, Inc.
Product code: Code MDB
Advisory panel: Microbiology
Date received: 1981-03-06
Decision date: 1981-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code MDB

product code MDB

Death: 6
Malfunction: 5,490
Total: 5,496

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.