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510(k) K933000

RECLINING GERI CHAIRS W/CASTERS & LAP TRAY by Winco, Inc. — Product Code INM

K933000 is an FDA 510(k) premarket notification submitted by Winco, Inc. for the device "RECLINING GERI CHAIRS W/CASTERS & LAP TRAY". The FDA issued a decision of Substantially Equivalent on September 30, 1993. The device falls under product code INM (Chair, With Casters), a Class I device regulated under 21 CFR 890.3100. Winco, Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1993
Date Received
June 18, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, With Casters
Device Class
Class I
Regulation Number
890.3100
Review Panel
PM
Submission Type

Other clearances by Winco, Inc.

  • K080533 — WINCO MODEL POWER SERIES LIFT CHAIR (August 11, 2008)
  • K941569 — CAREMOR CLINER (April 26, 1994)

Other clearances for product code INM

  • K063521 — NISSIN PEDIATRIC SERIES WHEELCHAIR (February 5, 2007)
  • K941738 — STRYKER 5050 STRECHAIR (May 6, 1994)
  • K941569 — CAREMOR CLINER (April 26, 1994)
  • K926028 — BENCHES (March 24, 1993)
  • K926025 — CHAIRS (March 22, 1993)
  • K926053 — ELD-ARONDAK CHAIR (March 22, 1993)
  • K926054 — ELD-ARONDAK CHAIR (March 22, 1993)
  • K924848 — KAYE SCOOT-ABOUT, MODEL SB1 (February 12, 1993)
  • K925247 — STONEHEART ROLLER AID (February 12, 1993)
  • K921917 — DOLOMITE ROLLATOR (May 26, 1992)

FDA data resources