510(k) K920451

ENDOTEK ULTRA SYSTEM by Surgitek — Product Code FAP

K920451 is an FDA 510(k) premarket notification submitted by Surgitek for the device "ENDOTEK ULTRA SYSTEM". The FDA issued a decision of Substantially Equivalent on September 17, 1992. The device falls under product code FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic Device), 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
September 17, 1992
Date Received
February 4, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
Device Class
Class II
Regulation Number
876.1620
Review Panel
GU
Submission Type