K-number	K960216
Device name	CPR SUCTION CATHETER KIT
Applicant	Custom Pack Reliability
Product code	JOL
Device class	Class II
Decision date	Apr 15, 1996
Decision	Substantially Equivalent
Regulation	880.6740

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Source

View the full FDA submission: accessdata.fda.gov

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CPR SUCTION CATHETER KIT

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