Home / 510(k) Clearances / K981032

510(k) K981032

PIV SYSTEM by Medical Solutions, Inc. — Product Code LDQ

K981032 is an FDA 510(k) premarket notification submitted by Medical Solutions, Inc. for the device "PIV SYSTEM". The FDA issued a decision of Substantially Equivalent on September 2, 1998. Medical Solutions, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 2, 1998
Date Received
March 19, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Medical Solutions, Inc.

  • K093689 — 1.5 TESLA 16- CHANNEL RECEIVE-ONLY PHASED- ARRAY HEAD COIL FOR SIEMANS (August 31, 2010)
  • K041839 — 8NONE (February 15, 2005)
  • K012276 — TEMP 3 (August 20, 2001)
  • K980086 — HEAT STACK (March 10, 1998)

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)
  • 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