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510(k) K882798

MULTIFLO ADAPTER by Deseret Medical, Inc. — Product Code FPA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 1988
Date Received
July 6, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type

Other clearances by Deseret Medical, Inc.

  • K913027 — VESSEL DILATOR (November 27, 1991)
  • K904648 — SAFE SYTE I.V. CATHETER PLACEMENT UNIT (December 14, 1990)
  • K904121 — VIALON OBTURATOR (November 8, 1990)
  • K904122 — INSYTE-A ARTERIAL CATHETERIZATION UNIT (October 4, 1990)
  • K900116 — DESERET OPTIMA INTRAVASCULAR CATHETER (June 18, 1990)
  • K895735 — DESERET MULTILUMEN SUBCLAVIAN CATHETER (May 18, 1990)
  • K895734 — DESERET INTRAVASCULAR CATHETER (April 9, 1990)
  • K894033 — DISPOSABLE CATHETER PRESSURE TRANSDUCER (October 17, 1989)
  • K893406 — DESERET PRN ADAPTER (June 22, 1989)
  • K882797 — LUER-LOK MULTIFLO ADAPTER (July 18, 1988)

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