K-number	K801982
Device name	THE MCSHIRLEY PERCUSSOR
Applicant	Mcshirley Products, Inc.
Product code	BYI
Device class	Class II
Decision date	Sep 16, 1980
Decision	Substantially Equivalent
Regulation	868.5665

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View the full FDA submission: accessdata.fda.gov

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THE MCSHIRLEY PERCUSSOR

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