K-number	K122047
Device name	ALAMO P
Applicant	Alliance Partners, LLC
Product code	MAX
Device class	Class II
Decision date	Sep 4, 2012
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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ALAMO P

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