K-number	K834614
Device name	WILCOR-XR RP-L MEDICAL FILM
Applicant	Cea America Corp.
Product code	IWZ
Device class	Class I
Decision date	Mar 5, 1984
Decision	Substantially Equivalent
Regulation	892.1840

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View the full FDA submission: accessdata.fda.gov

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WILCOR-XR RP-L MEDICAL FILM

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