AESCULAP STERILCONTAINER S— 510(k) K093493

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K093493 for AESCULAP STERILCONTAINER S, Substantially Equivalent on 2010-07-27. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code FRG
Advisory panel: General Hospital
Date received: 2009-11-10
Decision date: 2010-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

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.