K-number	K910307
Device name	CARDIOLAB AMPLIFIER MODULE (CAM)
Applicant	Prucka Engineering, Inc.
Product code	DRR
Device class	Class II
Decision date	Apr 12, 1991
Decision	Substantially Equivalent
Regulation	870.2050

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View the full FDA submission: accessdata.fda.gov

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CARDIOLAB AMPLIFIER MODULE (CAM)

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