CONTAINER SYSTEM— 510(k) K792558

Name: FDA 510(k) clearance K792558
Creator: U.S. Food and Drug Administration
Published: 1979-12-27

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K792558 for CONTAINER SYSTEM, Substantially Equivalent on 1979-12-27. Applicant: Aesculap Instruments Corp.. Device class: 2.

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code FLE
Device class: Class 2
Regulation: 21 CFR 880.6880
Advisory panel: General Hospital
Date received: 1979-12-12
Decision date: 1979-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.