K-number	K790746
Device name	THE BIONIC EXERCISER
Applicant	Scudder Molner Instruments
Product code	HCC
Device class	Class II
Decision date	May 14, 1979
Decision	Substantially Equivalent
Regulation	882.5050

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Source

View the full FDA submission: accessdata.fda.gov

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THE BIONIC EXERCISER

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