PRIMEVUE 21 3MP COLOR DISPLAY, MODEL AC-QX21-A9300— 510(k) K080320

Substantially Equivalent

Nds Surgical Imaging

FDA 510(k) clearance K080320 for PRIMEVUE 21 3MP COLOR DISPLAY, MODEL AC-QX21-A9300, Substantially Equivalent on 2008-02-21. Applicant: Nds Surgical Imaging.

Clearance details

Applicant: Nds Surgical Imaging
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2008-02-06
Decision date: 2008-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, 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.