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510(k) K885270

PERSONAL TRANSFER SYSTEM by Columbus Mckinnon Corp. — Product Code FNG

K885270 is an FDA 510(k) premarket notification submitted by Columbus Mckinnon Corp. for the device "PERSONAL TRANSFER SYSTEM". The FDA issued a decision of Substantially Equivalent on March 14, 1989. The device falls under product code FNG (Lift, Patient, Ac-Powered), a Class II device regulated under 21 CFR 880.5500.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 1989
Date Received
December 22, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lift, Patient, Ac-Powered
Device Class
Class II
Regulation Number
880.5500
Review Panel
HO
Submission Type

Other clearances for product code FNG

  • K121287 — HT-WEDGE (October 3, 2012)
  • K041503 — HOVERJACK AIR PATIENT LIFT DEVICE (August 12, 2004)
  • K940872 — PATIENT SUPPORT SYSTEM (October 13, 1994)
  • K935351 — A.C. POWER PATIENT LIFT (February 28, 1994)
  • K926411 — SAF-LIFT/SAF-KARY (March 31, 1993)
  • K912769 — PATIENT LIFT AND TRANSPORT (October 2, 1991)
  • K905414 — MANGAR BOOSTER (March 5, 1991)
  • K895677 — THE MURRAY MOBILIFT(TM) (October 26, 1990)
  • K903723 — BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F (September 24, 1990)
  • K896848 — LIFT MASTER PATIENT LIFT (May 29, 1990)

FDA data resources