K-number	K770968
Device name	MONITOR, PATIENT, MODEL PM-I0N
Applicant	Cavitron Corp.
Product code	CCK
Device class	Class II
Decision date	Jun 8, 1977
Decision	Substantially Equivalent
Regulation	868.1400

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Source

View the full FDA submission: accessdata.fda.gov

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MONITOR, PATIENT, MODEL PM-I0N

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