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510(k) K842342

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN by Med-West, Inc.

K842342 is an FDA 510(k) premarket notification submitted by Med-West, Inc. for the device "MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN". The FDA issued a decision of SESP on June 14, 1984. Med-West, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
June 14, 1984
Date Received
June 14, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Med-West, Inc.

  • K880877 — CONTRAST INJECTION DEVICE (May 31, 1988)
  • K880398 — POWER TOILET ELEVATOR (March 17, 1988)
  • K874470 — MWI 400 WOUND DRESSING (December 18, 1987)
  • K872724 — SHEATH/DILATORS (September 15, 1987)
  • K854612 — ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 (January 3, 1986)
  • K852162 — MNI 400 INJECTION CAPS (June 12, 1985)
  • K832124 — CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI (August 12, 1983)
  • K831828 — TEFLON FEMORAL CATHETER MWI 100,10 & (July 7, 1983)
  • K831401 — SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS (June 3, 1983)
  • K831440 — SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 (June 3, 1983)

FDA data resources