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510(k) K923364

TILT ADJUSTABLE SLIDING BACK RECLINE SEATING SYST by Labac Systems, Inc. — Product Code KNN

K923364 is an FDA 510(k) premarket notification submitted by Labac Systems, Inc. for the device "TILT ADJUSTABLE SLIDING BACK RECLINE SEATING SYST". The FDA issued a decision of Substantially Equivalent on March 22, 1993. The device falls under product code KNN (Components, Wheelchair), a Class I device regulated under 21 CFR 890.3920. Labac Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 1993
Date Received
July 8, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Components, Wheelchair
Device Class
Class I
Regulation Number
890.3920
Review Panel
PM
Submission Type

Other clearances by Labac Systems, Inc.

  • K941157 — BASIC RECLINE CHAIR (April 7, 1994)
  • K934418 — BASIC TILT CHAIR ( BTC ) (January 7, 1994)
  • K932639 — MANUAL TILT RECLINE CHAIR (MTC) (July 22, 1993)
  • K923362 — REDUCED SHEAR OWR RECLINE SYSTEM (March 26, 1993)
  • K923363 — ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM (March 24, 1993)
  • K921028 — MANUAL RECLINING CHAIR (March 24, 1993)
  • K925272 — PEDIATRIC TILT CHAIR (February 12, 1993)
  • K923366 — TILT SEATING SYSTEM (February 12, 1993)
  • K921136 — MANUAL TILT CHAIR (April 2, 1992)
  • K921027 — MANUAL CHAIR BASE (March 20, 1992)

Other clearances for product code KNN

  • K211919 — KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat (March 4, 2022)
  • K942311 — DYNASTY U1-33 AGM (November 7, 1994)
  • K942309 — DYNASTY U1-31 (GELL/CELL) (November 7, 1994)
  • K942310 — DYNASTY GC 12550 (GELL/CELL) (November 7, 1994)
  • K942308 — DYNASTY GC 12400 (GELL/CELL) (November 7, 1994)
  • K942312 — ALDEN LINEAGE WHEELCHAIR CUSHION (May 26, 1994)
  • K942260 — ALDEN WHEELCHAIR CUSHION (May 26, 1994)
  • K933051 — ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION (October 12, 1993)
  • K925980 — PM (March 24, 1993)
  • K923942 — RHOMBO MEDICAL RHOMBO-FILL (March 24, 1993)

FDA data resources