4 FRENCH & 5 FRENCH ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS MODELS 5UEXXX, 5BEXXX AND 5FEXXX, AND 4UEXXX, 4BEXXX AND 4FEX (K030852) — FDA 510(k) Clearance | Predicase

K-number	K030852
Device name	4 FRENCH & 5 FRENCH ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS MODELS 5UEXXX, 5BEXXX AND 5FEXXX, AND 4UEXXX, 4BEXXX AND 4FEX
Applicant	Mogul Enterprises
Product code	DRF
Device class	Class II
Decision date	Jul 10, 2003
Decision	Substantially Equivalent
Regulation	870.1220

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