510(k) K950498

LIFE TRACE TRANS TIP INTRAUTERINE PRESSURE CATHETER by Graphic Controls Corp. — Product Code KXO

K950498 is an FDA 510(k) premarket notification submitted by Graphic Controls Corp. for the device "LIFE TRACE TRANS TIP INTRAUTERINE PRESSURE CATHETER". The FDA issued a decision of Substantially Equivalent on July 24, 1995. The device falls under product code KXO (Monitor, Pressure, Intrauterine), a Class II device regulated under 21 CFR 884.2700. Graphic Controls Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 1995
Date Received
February 6, 1995
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