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510(k) K993797

EC-7701 FLUID WARMING CABINET by Enthermics Medical Systems, Inc. — Product Code LDQ

K993797 is an FDA 510(k) premarket notification submitted by Enthermics Medical Systems, Inc. for the device "EC-7701 FLUID WARMING CABINET". The FDA issued a decision of Substantially Equivalent on January 20, 2000. Enthermics Medical Systems, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 20, 2000
Date Received
November 9, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Enthermics Medical Systems, Inc.

  • K132202 — DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET (December 6, 2013)
  • K091336 — IVNOW MODULAR FLUID WARMER, 120V, MODEL IVNOW-1, IVNOW-2, IVNOW-3, IVNOW-6, IVNO (May 7, 2010)
  • K963731 — TRU-5000 THERMAL RECOVERY RADIANT HEATING UNIT (April 22, 1997)

Other clearances for product code LDQ

  • 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)
  • K934703 — MEDICOOL PROTECTALL (January 26, 1994)

FDA data resources