K-number	K960243
Device name	CPR C-SECTION DELIVERY PACK
Applicant	Custom Pack Reliability
Product code	MLS
Device class	Class II
Decision date	May 23, 1996
Decision	Substantially Equivalent
Regulation	884.4530

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Source

View the full FDA submission: accessdata.fda.gov

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CPR C-SECTION DELIVERY PACK

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