VENTED VIAL ADAPTER TRANSFER DEVICE— 510(k) K062482

Substantially Equivalent

Medimop Medical Projects, Ltd.

FDA 510(k) clearance K062482 for VENTED VIAL ADAPTER TRANSFER DEVICE, Substantially Equivalent on 2006-11-03. Applicant: Medimop Medical Projects, Ltd..

Clearance details

Applicant: Medimop Medical Projects, Ltd.
Product code: Code LHI
Advisory panel: General Hospital
Date received: 2006-08-24
Decision date: 2006-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raanana, IL

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Adverse events under product code LHI

product code LHI

Injury: 207
Malfunction: 7,820
Other: 3
Total: 8,030

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.