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510(k) K941569

CAREMOR CLINER by Winco, Inc. — Product Code INM

K941569 is an FDA 510(k) premarket notification submitted by Winco, Inc. for the device "CAREMOR CLINER". The FDA issued a decision of Substantially Equivalent on April 26, 1994. 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
April 26, 1994
Date Received
March 31, 1994
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)
  • K933000 — RECLINING GERI CHAIRS W/CASTERS & LAP TRAY (September 30, 1993)

Other clearances for product code INM

  • K063521 — NISSIN PEDIATRIC SERIES WHEELCHAIR (February 5, 2007)
  • K941738 — STRYKER 5050 STRECHAIR (May 6, 1994)
  • K933000 — RECLINING GERI CHAIRS W/CASTERS & LAP TRAY (September 30, 1993)
  • K926028 — BENCHES (March 24, 1993)
  • K926053 — ELD-ARONDAK CHAIR (March 22, 1993)
  • K926054 — ELD-ARONDAK CHAIR (March 22, 1993)
  • K926025 — CHAIRS (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