K-number	K000959
Device name	CRITERION 60 OR PM 60
Applicant	Caradyne, Ltd.
Product code	CAP
Device class	Class II
Decision date	Jun 22, 2000
Decision	Substantially Equivalent
Regulation	868.2600

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Source

View the full FDA submission: accessdata.fda.gov

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CRITERION 60 OR PM 60

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