AQUABOSS ECORO DIA I (HT); AQUABOSS ECORO DIA II (HT)— 510(k) K124059

Name: FDA 510(k) clearance K124059
Creator: U.S. Food and Drug Administration
Published: 2013-03-25

Substantially Equivalent

Lauer Membran Wassertechnik GmbH

FDA 510(k) clearance K124059 for AQUABOSS ECORO DIA I (HT); AQUABOSS ECORO DIA II (HT), Substantially Equivalent on 2013-03-25. Applicant: Lauer Membran Wassertechnik GmbH. Device class: 2.

Clearance details

Applicant: Lauer Membran Wassertechnik GmbH
Product code: Code FIP
Device class: Class 2
Regulation: 21 CFR 876.5665
Advisory panel: Gastroenterology, Urology
Date received: 2012-12-31
Decision date: 2013-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wittlingen, DE

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FIP

product code FIP

Malfunction: 490
Total: 490

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.