510(k) K881857

AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU. by Spectramed, Inc. — Product Code KXO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 1989
Date Received
May 3, 1988
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