K-number	K792601
Device name	LIFELIFT MODELS ONE AND TWO
Applicant	Corda Int'L Holiday, Inc.
Product code	FSA
Device class	Class I
Decision date	Dec 31, 1979
Decision	Substantially Equivalent
Regulation	880.5510

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Source

View the full FDA submission: accessdata.fda.gov

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LIFELIFT MODELS ONE AND TWO

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