K-number	K843389
Device name	CLINITRON AIR FLUIDIZED SUPPORT J-101UD
Applicant	Uhi Corp.
Product code	INX
Device class	Class II
Decision date	Sep 5, 1984
Decision	Substantially Equivalent
Regulation	890.5160

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View the full FDA submission: accessdata.fda.gov

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CLINITRON AIR FLUIDIZED SUPPORT J-101UD

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