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510(k) K884630

MULTI-PURPOSE HOLDER by Med-Dex Intl. — Product Code LDQ

K884630 is an FDA 510(k) premarket notification submitted by Med-Dex Intl. for the device "MULTI-PURPOSE HOLDER". The FDA issued a decision of Substantially Equivalent on November 22, 1988. Med-Dex Intl. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 22, 1988
Date Received
November 7, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Med-Dex Intl.

  • K893569 — QUICK CHANGE MONTGOMERY STRAP (September 25, 1989)
  • K881083 — GENERAL PURPOSE KIT (April 7, 1988)
  • K881084 — UTILITY CLAMP (March 25, 1988)

Other clearances for product code LDQ

  • K993797 — EC-7701 FLUID WARMING CABINET (January 20, 2000)
  • K992258 — HOT SHOT FLUID WARMER IV FLUIDS (January 12, 2000)
  • K981032 — PIV SYSTEM (September 2, 1998)
  • K973747 — CONTROLLED TEMPERATURE CABINET SYSTEM (May 7, 1998)
  • K955661 — ACU-HALT (December 30, 1996)
  • K955776 — ACU-LAB (June 5, 1996)
  • K945374 — ACU-HALT (August 9, 1995)
  • K944961 — PERSONAL ALARM SYSTEM (PAS) (August 7, 1995)
  • K942810 — PALCO LABS COLD POUCH (June 28, 1995)
  • K930884 — MEDICAL PROCEDURE TRAY, MODIFICATION (March 21, 1995)

FDA data resources