K-number	K953507
Device name	TYPE 1 & 2 (HUMIDAIR I & II)
Applicant	Icor AB
Product code	BYD
Device class	Class I
Decision date	Sep 7, 1995
Decision	Substantially Equivalent
Regulation	868.5375

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View the full FDA submission: accessdata.fda.gov

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TYPE 1 & 2 (HUMIDAIR I & II)

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