510(k) K920030

SURESEAL ENDOSCOPIC VALVE by Applied Urology, Inc. — Product Code ODC

K920030 is an FDA 510(k) premarket notification submitted by Applied Urology, Inc. for the device "SURESEAL ENDOSCOPIC VALVE". The FDA issued a decision of Substantially Equivalent on March 18, 1992. The device falls under product code ODC (Endoscope Channel Accessory), a Class II device regulated under 21 CFR 876.1500. Applied Urology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 1992
Date Received
January 3, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscope Channel Accessory
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To give the endoscope channel additional or improved functionality.