K-number	K813123
Device name	EPC FILTER
Applicant	Codman & Shurtleff, Inc.
Product code	DRR
Device class	Class II
Decision date	Nov 27, 1981
Decision	Substantially Equivalent
Regulation	870.2050

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Source

View the full FDA submission: accessdata.fda.gov

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EPC FILTER

Everything you need for a 510(k) submission. Nothing you don't.