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510(k) K823206

MARTIN PELVIC LIFT by Martin Pelvic Lift Co. — Product Code FSA

K823206 is an FDA 510(k) premarket notification submitted by Martin Pelvic Lift Co. for the device "MARTIN PELVIC LIFT". The FDA issued a decision of Substantially Equivalent on April 28, 1983. The device falls under product code FSA (Lift, Patient, Non-Ac-Powered), a Class I device regulated under 21 CFR 880.5510.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 28, 1983
Date Received
October 27, 1982
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 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)
  • K844976 — MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT (April 1, 1985)
  • K841395 — SHOWER TROLLEY (May 7, 1984)
  • K841398 — VARIABLE HEIGHT TRANSFER CHAIR (May 7, 1984)
  • K840997 — BATTERY POWERED PATIENT LIFT (April 17, 1984)
  • K811899 — CENTURY LIFT TRANSFER SYSTEM (July 23, 1981)

FDA data resources