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510(k) K903905

SERIES 9000 LIFT-RECLINE CHAIR by Equi-Tron Mfg., Inc. — Product Code INO

K903905 is an FDA 510(k) premarket notification submitted by Equi-Tron Mfg., Inc. for the device "SERIES 9000 LIFT-RECLINE CHAIR". The FDA issued a decision of Substantially Equivalent on September 17, 1990. The device falls under product code INO (Chair, Positioning, Electric), a Class II device regulated under 21 CFR 890.3110. Equi-Tron Mfg., Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 17, 1990
Date Received
August 23, 1990
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 Equi-Tron Mfg., Inc.

  • K962763 — 2000 MODULAR THIRTY-NINE (October 7, 1996)
  • K903904 — SERIES 2000 ADJUSTABLE BED (October 12, 1990)
  • K902089 — EQUI-GUARD (ASPIRATOR FILTER) (July 6, 1990)
  • K894831 — PORTABLE AIR COMPRESSOR MODEL NUMBER 8125 (October 24, 1989)

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