K-number	K892123
Device name	GOETTINGER EMERGENCY RESUSCITATION TUBE
Applicant	Plastic Parts Corp.
Product code	CAE
Device class	Class I
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	868.5110

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View the full FDA submission: accessdata.fda.gov

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GOETTINGER EMERGENCY RESUSCITATION TUBE

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