K-number	K871864
Device name	PB240 PATIENT MONITOR/PULSE OXIMETER
Applicant	Puritan Bennett Corp.
Product code	DQA
Device class	Class II
Decision date	Jun 24, 1987
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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PB240 PATIENT MONITOR/PULSE OXIMETER

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