K-number	K051751
Device name	EQUA-PULL SAFETY RELEASE MODULE
Applicant	Ortho Technology
Product code	DZB
Device class	Class II
Decision date	Jul 22, 2005
Decision	Substantially Equivalent
Regulation	872.5500

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View the full FDA submission: accessdata.fda.gov

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EQUA-PULL SAFETY RELEASE MODULE

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