DIGI -FLOW— 510(k) K920671

Substantially Equivalent

D and D Technology, Inc.

FDA 510(k) clearance K920671 for DIGI -FLOW, Substantially Equivalent on 1993-01-28. Applicant: D and D Technology, Inc..

Clearance details

Applicant: D and D Technology, Inc.
Product code: Code KOC
Advisory panel: Gastroenterology, Urology
Date received: 1992-02-13
Decision date: 1993-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo, NY, US

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Adverse events under product code KOC

product code KOC

Death: 4
Total: 4

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.