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510(k) K895932

PSG(TM) EDM(TM) INFUSION CATHETER by Peripheral Systems Group — Product Code DQY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 4, 1990
Date Received
October 10, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Percutaneous
Device Class
Class II
Regulation Number
870.1250
Review Panel
CV
Submission Type

Other clearances by Peripheral Systems Group

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  • K934433 — VANTAGE DIALTAION CATHETER (December 9, 1993)
  • K932777 — SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER (October 7, 1993)
  • K931327 — PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE (July 14, 1993)
  • K915554 — HI-TORQUE SPORT-T(TM) GUIDE WIRE (February 9, 1993)
  • K914979 — EDM(R) INFUSION CATHETER (September 16, 1992)
  • K913941 — PSG(TM) 20 GUAGE DOPPLER NEEDLE (February 27, 1992)
  • K915168 — PROFLEX 5 (February 19, 1992)
  • K913477 — APEX(TM) PROSTATIC BALLOON DILATION CATHETER (December 27, 1991)
  • K913746 — SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM (December 17, 1991)

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