SPIROSAFE FILTER— 510(k) K973314

Substantially Equivalent

Micro Direct, Inc.

FDA 510(k) clearance K973314 for SPIROSAFE FILTER, Substantially Equivalent on 1997-11-21. Applicant: Micro Direct, Inc..

Clearance details

Applicant: Micro Direct, Inc.
Product code: Code CAH
Advisory panel: Anesthesiology
Date received: 1997-09-03
Decision date: 1997-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lewiston, ME, US

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Adverse events under product code CAH

product code CAH

Death: 7
Total: 7

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.