K-number	K960194
Device name	MYELOTEC MYELOSCOPE
Applicant	Myelotec, Inc.
Product code	HRX
Device class	Class II
Decision date	Sep 4, 1996
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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MYELOTEC MYELOSCOPE

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