K-number	K925325
Device name	A-DEC 2185 DOCTOR'S UNIT
Applicant	A-Dec, Inc.
Product code	KLC
Device class	Class I
Decision date	Dec 9, 1993
Decision	Substantially Equivalent
Regulation	872.6250

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View the full FDA submission: accessdata.fda.gov

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A-DEC 2185 DOCTOR'S UNIT

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