SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM— 510(k) K072511

Substantially Equivalent

Medimop Medical Projects, Ltd.

FDA 510(k) clearance K072511 for SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM, Substantially Equivalent on 2007-12-13. Applicant: Medimop Medical Projects, Ltd..

Clearance details

Applicant: Medimop Medical Projects, Ltd.
Product code: Code LHI
Advisory panel: General Hospital
Date received: 2007-09-06
Decision date: 2007-12-13
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Lionville, PA, US

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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.