PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.— 510(k) K896680

Substantially Equivalent

Interson Corp.

FDA 510(k) clearance K896680 for PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC., Substantially Equivalent on 1990-02-14. Applicant: Interson Corp..

Clearance details

Applicant: Interson Corp.
Product code: Code FED
Advisory panel: Gastroenterology, Urology
Date received: 1989-11-27
Decision date: 1990-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FED

product code FED

Death: 10
Total: 10

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.