510(k) K952527

BALLOON UTERINE STENT by Cook Urological, Inc. — Product Code KNA

K952527 is an FDA 510(k) premarket notification submitted by Cook Urological, Inc. for the device "BALLOON UTERINE STENT". The FDA issued a decision of Substantially Equivalent on January 2, 1996. The device falls under product code KNA (Instrument, Manual, Specialized Obstetric-Gynecologic), a Class II device regulated under 21 CFR 884.4530. Cook Urological, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 2, 1996
Date Received
June 1, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Manual, Specialized Obstetric-Gynecologic
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type