MEDISYSTEMS ANTI-STICK INJECTION SITE NEEDLE— 510(k) K910733

Substantially Equivalent

Medisystems Corp.

FDA 510(k) clearance K910733 for MEDISYSTEMS ANTI-STICK INJECTION SITE NEEDLE, Substantially Equivalent on 1991-06-06. Applicant: Medisystems Corp..

Clearance details

Applicant: Medisystems Corp.
Product code: Code FMI
Advisory panel: General Hospital
Date received: 1991-02-21
Decision date: 1991-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

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Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.