510(k) K952527
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