K-number	K822286
Device name	AUTOCUFF (PHOTOS ENCLOSED WITH 510K
Applicant	Partamed, Inc.
Product code	KZD
Device class	Class I
Decision date	Aug 27, 1982
Decision	Substantially Equivalent
Regulation	880.5420

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View the full FDA submission: accessdata.fda.gov

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AUTOCUFF (PHOTOS ENCLOSED WITH 510K

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