K-number	K952325
Device name	ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
Applicant	Icor AB
Product code	CCK
Device class	Class II
Decision date	Jul 31, 1995
Decision	Substantially Equivalent
Regulation	868.1400

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View the full FDA submission: accessdata.fda.gov

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ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)

Everything you need for a 510(k) submission. Nothing you don't.