K-number	K810731
Device name	MODEL IM1000 INTEGRATED MONITOR
Applicant	Gould, Inc.
Product code	DQK
Device class	Class II
Decision date	Mar 27, 1981
Decision	Substantially Equivalent
Regulation	870.1425

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View the full FDA submission: accessdata.fda.gov

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MODEL IM1000 INTEGRATED MONITOR

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