510(k) K090762 · GEX Powered Laser Surgical Instrument

LEDA

Applicant	Quantel Derma GmbH, Erlangen, DE
Decision	Substantially Equivalent, Aug 28, 2009
Received	Mar 23, 2009
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K090762

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.