K-number	K051904
Device name	ALL PURPOSE CUFF, MODEL 222APC
Applicant	Suntech Medical, Inc.
Product code	DXQ
Device class	Class II
Decision date	Sep 9, 2005
Decision	Substantially Equivalent
Regulation	870.1120

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View the full FDA submission: accessdata.fda.gov

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ALL PURPOSE CUFF, MODEL 222APC

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