INITARY BETTER BLADDER-PEDIATRIC— 510(k) K140321

Name: FDA 510(k) clearance K140321
Creator: U.S. Food and Drug Administration
Published: 2014-04-17

Substantially Equivalent

Circulatory Technology, Inc.

FDA 510(k) clearance K140321 for INITARY BETTER BLADDER-PEDIATRIC, Substantially Equivalent on 2014-04-17. Applicant: Circulatory Technology, Inc.. Device class: 2.

Clearance details

Applicant: Circulatory Technology, Inc.
Product code: Code DTN
Device class: Class 2
Regulation: 21 CFR 870.4400
Advisory panel: Cardiovascular
Date received: 2014-02-18
Decision date: 2014-04-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Oyster Bay, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DTN

product code DTN

Death: 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.