MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP— 510(k) K081463

Substantially Equivalent

Medel S.P.A.

FDA 510(k) clearance K081463 for MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP, Substantially Equivalent on 2009-02-06. Applicant: Medel S.P.A..

Clearance details

Applicant: Medel S.P.A.
Product code: Code HGX
Advisory panel: Obstetrics/Gynecology
Date received: 2008-05-23
Decision date: 2009-02-06
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Cary, NC, US

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Adverse events under product code HGX

product code HGX

Injury: 758
Other: 2
Total: 760

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.