ZINETICS INTERNAL REFERENCE PROBE— 510(k) K910694

Substantially Equivalent

Zinetics Medical, Inc.

FDA 510(k) clearance K910694 for ZINETICS INTERNAL REFERENCE PROBE, Substantially Equivalent on 1991-05-17. Applicant: Zinetics Medical, Inc..

Clearance details

Applicant: Zinetics Medical, Inc.
Product code: Code FFT
Advisory panel: Gastroenterology, Urology
Date received: 1991-02-19
Decision date: 1991-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code FFT

product code FFT

Injury: 595
Malfunction: 2,175
Other: 1
Total: 2,771

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.