KEYMED FLEXIBLE ESOPHAGEAL DILATORS— 510(k) K862000

Substantially Equivalent

Keymed, Inc.

FDA 510(k) clearance K862000 for KEYMED FLEXIBLE ESOPHAGEAL DILATORS, Substantially Equivalent on 1986-08-12. Applicant: Keymed, Inc..

Clearance details

Applicant: Keymed, Inc.
Product code: Code KNQ
Advisory panel: Gastroenterology, Urology
Date received: 1986-05-23
Decision date: 1986-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Essex Ss2 5qh England, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNQ

product code KNQ

Malfunction: 1,844
Total: 1,844

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.