K-number	K936009
Device name	AMS 3000M
Applicant	Acutronic Medical Systems AG
Product code	CAP
Device class	Class II
Decision date	May 3, 1995
Decision	Substantially Equivalent
Regulation	868.2600

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View the full FDA submission: accessdata.fda.gov

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AMS 3000M

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