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510(k) K883309

MULTI-CARE CHAIR by Mid-Canada Medical — Product Code INM

K883309 is an FDA 510(k) premarket notification submitted by Mid-Canada Medical for the device "MULTI-CARE CHAIR". The FDA issued a decision of Substantially Equivalent on September 30, 1988. The device falls under product code INM (Chair, With Casters), a Class I device regulated under 21 CFR 890.3100. Mid-Canada Medical has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1988
Date Received
August 5, 1988
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 Mid-Canada Medical

  • K933237 — MEDI-STIM, MODIFICATION (September 8, 1994)
  • K922839 — MID-CANADA MEDICAL (July 2, 1993)
  • K921491 — MEDI-STIM (September 3, 1992)
  • K883308 — PARKER BATHING SYSTEM (September 22, 1988)

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)
  • K933000 — RECLINING GERI CHAIRS W/CASTERS & LAP TRAY (September 30, 1993)
  • K926028 — BENCHES (March 24, 1993)
  • K926053 — ELD-ARONDAK CHAIR (March 22, 1993)
  • K926025 — CHAIRS (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)

FDA data resources