K-number	K014160
Device name	PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)
Applicant	Cook Urological, Inc.
Product code	MQG
Device class	Class II
Decision date	Feb 8, 2002
Decision	Substantially Equivalent
Regulation	884.6120

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View the full FDA submission: accessdata.fda.gov

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PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)

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