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510(k) K895677

THE MURRAY MOBILIFT(TM) by Medical/Surgical Specialties, Ltd. — Product Code FNG

K895677 is an FDA 510(k) premarket notification submitted by Medical/Surgical Specialties, Ltd. for the device "THE MURRAY MOBILIFT(TM)". The FDA issued a decision of Substantially Equivalent on October 26, 1990. The device falls under product code FNG (Lift, Patient, Ac-Powered), a Class II device regulated under 21 CFR 880.5500. Medical/Surgical Specialties, Ltd. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 26, 1990
Date Received
September 20, 1989
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 by Medical/Surgical Specialties, Ltd.

  • K900633 — DISP. ELECTROSURGERY PENCIL, HAND CONTROL (May 7, 1990)
  • K881392 — CARDICAD(TM) (May 31, 1988)
  • K881427 — SPIRIX(TM) (April 19, 1988)

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)
  • K903723 — BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F (September 24, 1990)
  • K896848 — LIFT MASTER PATIENT LIFT (May 29, 1990)
  • K885270 — PERSONAL TRANSFER SYSTEM (March 14, 1989)

FDA data resources