510(k) K896122

AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED by Spectramed, Inc. — Product Code KXO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 19, 1990
Date Received
October 24, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Pressure, Intrauterine
Device Class
Class II
Regulation Number
884.2700
Review Panel
OB
Submission Type