K-number	K853240
Device name	MERIDIAN ULTRASOUND IMAGING SYSTEM
Applicant	Johnson & Johnson Professionals, Inc.
Product code	JOP
Device class	Class II
Decision date	Feb 21, 1986
Decision	Substantially Equivalent
Regulation	870.2880

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View the full FDA submission: accessdata.fda.gov

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MERIDIAN ULTRASOUND IMAGING SYSTEM

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