SMARTLOCK SAFETY SYRINGE— 510(k) K973888

Substantially Equivalent

Medical Innovation , Ltd.

FDA 510(k) clearance K973888 for SMARTLOCK SAFETY SYRINGE, Substantially Equivalent on 1998-06-03. Applicant: Medical Innovation , Ltd..

Clearance details

Applicant: Medical Innovation , Ltd.
Product code: Code MEG
Advisory panel: General Hospital
Date received: 1997-10-14
Decision date: 1998-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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Adverse events under product code MEG

product code MEG

Malfunction: 1,373
Other: 1
Total: 1,374

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.