ENDURAMESH, MODEL 762.XXX (K093207) — FDA 510(k) Clearance | Predicase

K-number	K093207
Device name	ENDURAMESH, MODEL 762.XXX
Applicant	Lucero Medical, LLC
Product code	MQP
Device class	Class II
Decision date	Apr 26, 2010
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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