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LEDA — Quantel Derma GmbH (510(k) K090762)

LEDA — Quantel Derma GmbH (510(k) K090762) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LEDA; Applicant: Quantel Derma GmbH; Clearance track: 510(k).

Device nameLEDA
ApplicantQuantel Derma GmbH
Clearance track510(k)
Submission numberK090762
DecisionSubstantially Equivalent
Decision date2009-08-28
Date received2009-03-23
Product codeGEX
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationDE
SourceopenFDA device

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