Astell UMB 220, UMB 230, UMB 240 Autoclaves/sterilizers— 510(k) K170304

Name: FDA 510(k) clearance K170304
Creator: U.S. Food and Drug Administration
Published: 2018-03-02

Substantially Equivalent

Astell Scientific Limited

FDA 510(k) clearance K170304 for Astell UMB 220, UMB 230, UMB 240 Autoclaves/sterilizers, Substantially Equivalent on 2018-03-02. Applicant: Astell Scientific Limited. Device class: 2.

Clearance details

Applicant: Astell Scientific Limited
Product code: Code FLE
Device class: Class 2
Regulation: 21 CFR 880.6880
Advisory panel: General Hospital
Date received: 2017-01-31
Decision date: 2018-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sidcup, GB

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.