K-number	K033904
Device name	PRE-IMPLANTATION GENETIC DIAGNOSIS PIPETTES (BIOPSY PIPETTES)
Applicant	Cook Urological, Inc.
Product code	MQH
Device class	Class II
Decision date	Jan 16, 2004
Decision	Substantially Equivalent
Regulation	884.6130

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View the full FDA submission: accessdata.fda.gov

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PRE-IMPLANTATION GENETIC DIAGNOSIS PIPETTES (BIOPSY PIPETTES)

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