FLEX-I-GRASP— 510(k) K854889

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K854889 for FLEX-I-GRASP, Substantially Equivalent on 1986-02-21. Applicant: Euro-Med Intl..

Clearance details

Applicant: Euro-Med Intl.
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 1985-12-06
Decision date: 1986-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

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Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.