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510(k) K930625

SANITAS PATIENT LIFT by Dutton-Lainson Co. — Product Code FSA

K930625 is an FDA 510(k) premarket notification submitted by Dutton-Lainson Co. for the device "SANITAS PATIENT LIFT". The FDA issued a decision of Substantially Equivalent on September 13, 1993. The device falls under product code FSA (Lift, Patient, Non-Ac-Powered), a Class I device regulated under 21 CFR 880.5510. Dutton-Lainson Co. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 13, 1993
Date Received
February 8, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lift, Patient, Non-Ac-Powered
Device Class
Class I
Regulation Number
880.5510
Review Panel
HO
Submission Type

Other clearances by Dutton-Lainson Co.

  • K930624 — SANITAS WHIRPOOL BATHING SYSTEM (July 1, 1994)
  • K930626 — SANITAS PATIENT SCALE (August 6, 1993)

Other clearances for product code FSA

  • K942807 — SURGICAL LIFT SHEET (August 2, 1994)
  • K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY (September 12, 1990)
  • K860837 — HOYER ONE-TOUCH POWER LIFTER (March 27, 1986)
  • K851844 — MOLIFT (May 17, 1985)
  • K844976 — MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT (April 1, 1985)
  • K841398 — VARIABLE HEIGHT TRANSFER CHAIR (May 7, 1984)
  • K841395 — SHOWER TROLLEY (May 7, 1984)
  • K840997 — BATTERY POWERED PATIENT LIFT (April 17, 1984)
  • K823206 — MARTIN PELVIC LIFT (April 28, 1983)
  • K811899 — CENTURY LIFT TRANSFER SYSTEM (July 23, 1981)

FDA data resources