510(k) K983593

OVUM PICK-UP ASPIRATION NEEDLES by Cook Ob/Gyn — Product Code MQE

K983593 is an FDA 510(k) premarket notification submitted by Cook Ob/Gyn for the device "OVUM PICK-UP ASPIRATION NEEDLES". The FDA issued a decision of Substantially Equivalent on January 21, 1999. The device falls under product code MQE (Needle, Assisted Reproduction), a Class II device regulated under 21 CFR 884.6100. Cook Ob/Gyn has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1999
Date Received
October 13, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Assisted Reproduction
Device Class
Class II
Regulation Number
884.6100
Review Panel
OB
Submission Type