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510(k) K880800

GOLDEN POWER LIFT CHAIR by Golden Technologies, Inc. — Product Code INO

K880800 is an FDA 510(k) premarket notification submitted by Golden Technologies, Inc. for the device "GOLDEN POWER LIFT CHAIR". The FDA issued a decision of Substantially Equivalent on March 14, 1988. The device falls under product code INO (Chair, Positioning, Electric), a Class II device regulated under 21 CFR 890.3110. Golden Technologies, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 1988
Date Received
February 29, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Positioning, Electric
Device Class
Class II
Regulation Number
890.3110
Review Panel
PM
Submission Type

Other clearances by Golden Technologies, Inc.

  • K063162 — GOLDEN LITEWAY (November 2, 2006)
  • K041341 — GOLDEN SPYDER, MODEL GS-300 (June 3, 2004)
  • K041025 — BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELED (May 3, 2004)
  • K012258 — COMPANION MODEL 221, 321, 421 (December 3, 2001)
  • K011153 — ALANTE, BATTERY OPERATED POWER WHEELCHAIR (May 29, 2001)
  • K971043 — GOLDEN EAGLE (August 1, 1997)
  • K971050 — GOLDEN HAWK (August 1, 1997)

Other clearances for product code INO

  • K131909 — DALTON LIFT CHAIR (February 24, 2014)
  • K123834 — EASYSTAND BANTAM MEDIUM (August 13, 2013)
  • K112944 — FRESENIUS MEDICAL TREATMENT CHAIR T688 SERIES (December 30, 2011)
  • K101723 — COMPACT WHEELCHAIR PLATFORM (December 23, 2010)
  • K091578 — LIFT CHAIR, MODEL T3 (December 2, 2009)
  • K091242 — BANTAM (July 6, 2009)
  • K091727 — MEDICAL TREATMENT CHAIR, T400, T500,T600 (July 6, 2009)
  • K073565 — STANDARD WHEELCHAIR PLATFORM (February 6, 2009)
  • K081053 — PIVOT ASSIST (October 9, 2008)
  • K080533 — WINCO MODEL POWER SERIES LIFT CHAIR (August 11, 2008)

FDA data resources