510(k) K944391

OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM by Surgitek — Product Code FEN

K944391 is an FDA 510(k) premarket notification submitted by Surgitek for the device "OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM". The FDA issued a decision of Substantially Equivalent on February 7, 1995. The device falls under product code FEN (Device, Cystometric, Hydraulic), a Class II device regulated under 21 CFR 876.1620. Surgitek has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1995
Date Received
September 9, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Cystometric, Hydraulic
Device Class
Class II
Regulation Number
876.1620
Review Panel
GU
Submission Type