K-number	K963198
Device name	PS-41 6M PATIENT SIMULATOR
Applicant	Metron U.S., Inc.
Product code	DPS
Device class	Class II
Decision date	Mar 5, 1997
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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PS-41 6M PATIENT SIMULATOR

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