K-number	K922817
Device name	PM3000 & PM3100 VACUUM REGULATOR
Applicant	Precision Medical, Inc.
Product code	KDP
Device class	Class II
Decision date	Mar 4, 1993
Decision	Substantially Equivalent
Regulation	880.6740

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View the full FDA submission: accessdata.fda.gov

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PM3000 & PM3100 VACUUM REGULATOR

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