MEDEVIEW SYSTEM— 510(k) K002789

Substantially Equivalent

Medeview.Com

FDA 510(k) clearance K002789 for MEDEVIEW SYSTEM, Substantially Equivalent on 2001-03-21. Applicant: Medeview.Com.

Clearance details

Applicant: Medeview.Com
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2000-09-07
Decision date: 2001-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walthan, MA, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.