510(k) K020301— MODIFICATION TO VISTA STEREOSCOPE SYSTEM

Substantially Equivalent

Vista Medical Technologies, Inc.

Clearance details

Applicant: Vista Medical Technologies, Inc.
Product code: Code FET
Advisory panel: Gastroenterology, Urology
Date received: 2002-01-29
Decision date: 2002-02-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Westborough, MA, US

Adverse events under product code FET

product code FET

Injury: 313
Malfunction: 54,276
Total: 54,589

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.