LIQUIBAND DUAL, MODEL LBD 001— 510(k) K102076

Substantially Equivalent

Medlogic Global Limited

FDA 510(k) clearance K102076 for LIQUIBAND DUAL, MODEL LBD 001, Substantially Equivalent on 2011-02-18. Applicant: Medlogic Global Limited.

Clearance details

Applicant: Medlogic Global Limited
Product code: Code MPN
Advisory panel: General, Plastic Surgery
Date received: 2010-07-26
Decision date: 2011-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plympton, Plymouth, Devon, GB

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Adverse events under product code MPN

product code MPN

Injury: 856
Other: 1
Total: 857

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.