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LIQUIBAND DUAL, MODEL LBD 001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102076
510(k) Type
Traditional
Applicant
Medlogic Global Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/18/2011
Days to Decision
207 days
Submission Type
Summary

LIQUIBAND DUAL, MODEL LBD 001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102076
510(k) Type
Traditional
Applicant
Medlogic Global Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/18/2011
Days to Decision
207 days
Submission Type
Summary