510(k) K913169

DANTEC UD 5500 MK2 by Dantec Medical, Inc. — Product Code FAP

K913169 is an FDA 510(k) premarket notification submitted by Dantec Medical, Inc. for the device "DANTEC UD 5500 MK2". The FDA issued a decision of Substantially Equivalent on January 23, 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. Dantec Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1992
Date Received
July 17, 1991
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