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510(k) K900459

APPLICARD (EKG) by Medi-Globe Corp. — Product Code DRY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 31, 1990
Date Received
January 30, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4330
Review Panel
CV
Submission Type

Other clearances by Medi-Globe Corp.

  • K061222 — INJECTRA INJECTION NEEDLE (July 3, 2006)
  • K051247 — SONOTIP II ULTRASOUND NEEDLE SYSTEM (June 16, 2005)
  • K011261 — STONE EXTRACTOR BALLOON CATHETER (November 17, 2003)
  • K010714 — EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830 (January 21, 2003)
  • K010549 — BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS) (January 18, 2002)
  • K990220 — MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM (March 31, 1999)
  • K953355 — GIP/MEID-GLOBE HOT BIOPSY FORCEPS (April 4, 1996)
  • K955558 — GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES (February 29, 1996)
  • K953827 — GIP/MEDI-GLOBE ERCP CATHETERS (September 1, 1995)
  • K941973 — GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES (June 30, 1995)

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  • K133157 — TRI-OPTIC MEASUREMENT CELL; WITH BALANCE BIOSURFACE, WITH CARMEDA BIOACTIVE SURF (October 23, 2014)
  • K133658 — CDI BLOOD PARAMETER MONITORING SYSTEM 500 (July 25, 2014)
  • K123039 — CDI BLOOD PARAMETER MONITORING SYSTEM 500 (November 20, 2012)