K-number	K893420
Device name	MASTERLAB PFT AND MASTERLAB BODY BOX
Applicant	Quinton, Inc.
Product code	CCM
Device class	Class II
Decision date	Jun 23, 1989
Decision	Substantially Equivalent
Regulation	868.1750

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View the full FDA submission: accessdata.fda.gov

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MASTERLAB PFT AND MASTERLAB BODY BOX

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