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510(k) K844976

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT by Medi-Man Rehabilitation Products, Inc. — Product Code FSA

K844976 is an FDA 510(k) premarket notification submitted by Medi-Man Rehabilitation Products, Inc. for the device "MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT". The FDA issued a decision of Substantially Equivalent on April 1, 1985. The device falls under product code FSA (Lift, Patient, Non-Ac-Powered), a Class I device regulated under 21 CFR 880.5510. Medi-Man Rehabilitation Products, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1985
Date Received
December 26, 1984
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 Medi-Man Rehabilitation Products, Inc.

  • K992779 — A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM (January 13, 2000)
  • K925195 — MALIBU BATHING SYSTEM (October 17, 1994)
  • K924905 — MEDI-PLINTH (February 16, 1993)

Other clearances for product code FSA

  • K942807 — SURGICAL LIFT SHEET (August 2, 1994)
  • K930625 — SANITAS PATIENT LIFT (September 13, 1993)
  • K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY (September 12, 1990)
  • K860837 — HOYER ONE-TOUCH POWER LIFTER (March 27, 1986)
  • K851844 — MOLIFT (May 17, 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