K-number	K020421
Device name	GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES
Applicant	Hennig Enterprises Europe Srl
Product code	MEA
Device class	Class II
Decision date	Apr 29, 2003
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

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