K-number	K020337
Device name	READI-STRAND; MODEL PSSTRAND
Applicant	Worldwide Medical Technologies, LLC
Product code	KXK
Device class	Class II
Decision date	Jul 29, 2002
Decision	Substantially Equivalent
Regulation	892.5730

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View the full FDA submission: accessdata.fda.gov

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READI-STRAND; MODEL PSSTRAND

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