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510(k) K891023

SIEMENS CEILING STAND 800F, 800 AND 810 by Siemens Medical Electronics — Product Code LDQ

K891023 is an FDA 510(k) premarket notification submitted by Siemens Medical Electronics for the device "SIEMENS CEILING STAND 800F, 800 AND 810". The FDA issued a decision of Substantially Equivalent on July 25, 1989. Siemens Medical Electronics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 25, 1989
Date Received
February 28, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Siemens Medical Electronics

  • K935043 — SIEMENS CLINICAL WORK STATION (April 7, 1995)
  • K921930 — SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI (May 7, 1993)
  • K920445 — SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIES (March 2, 1993)
  • K914765 — SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYS (November 6, 1992)
  • K912070 — SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT (April 23, 1992)
  • K913489 — SIEMENS MICRO2 PULSE OXIMETER (October 30, 1991)
  • K905775 — SIEMENS ETCO2 CARTRIDGE (March 11, 1991)
  • K900319 — SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM (June 28, 1990)
  • K901771 — SIEMENS SIRECUST 732, PATIENT MONITOR (May 30, 1990)
  • K894460 — SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA (October 2, 1989)

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