HEMOPHRON— 510(k) K810612

Substantially Equivalent

Renal Devices, Inc.

FDA 510(k) clearance K810612 for HEMOPHRON, Substantially Equivalent on 1981-04-29. Applicant: Renal Devices, Inc..

Clearance details

Applicant: Renal Devices, Inc.
Product code: Code FKQ
Advisory panel: Gastroenterology, Urology
Date received: 1981-03-06
Decision date: 1981-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FKQ

product code FKQ

Other: 1
Total: 1

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.