K-number	K840963
Device name	SD PLUS PATIENT CAT.#78-8010
Applicant	Codman & Shurtleff, Inc.
Product code	GZJ
Device class	Class II
Decision date	Apr 23, 1984
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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SD PLUS PATIENT CAT.#78-8010

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