K-number	K910833
Device name	COLOR VUE TM- MYCOPLASMA PNEUMONIAE
Applicant	Seradyn, Inc.
Product code	GSA
Device class	Class I
Decision date	Jun 24, 1991
Decision	Substantially Equivalent
Regulation	866.3375

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View the full FDA submission: accessdata.fda.gov

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COLOR VUE TM- MYCOPLASMA PNEUMONIAE

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