CUTTER RESIFLEX URINE METER— 510(k) K781521

Name: FDA 510(k) clearance K781521
Creator: U.S. Food and Drug Administration
Published: 1978-11-22

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K781521 for CUTTER RESIFLEX URINE METER, Substantially Equivalent on 1978-11-22. Applicant: Cutter Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code KNX
Device class: Class 2
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1978-09-05
Decision date: 1978-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KNX

product code KNX

Malfunction: 1,064
Total: 1,064

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.