K-number	K901223
Device name	VACUUM ERECTION DEVICE (VED)
Applicant	Mission Pharmacal Co.
Product code	LKY
Device class	Class II
Decision date	May 4, 1990
Decision	Substantially Equivalent
Regulation	876.5020

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View the full FDA submission: accessdata.fda.gov

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VACUUM ERECTION DEVICE (VED)

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