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510(k) K792601

Device
LIFELIFT MODELS ONE AND TWO
Applicant
CORDA INT'L HOLIDAY, INC.
510(k) number
K792601
Product code
FSA  
Decision
Substantially Equivalent (SESE)
Decision date
1979-12-31
Date received
1979-12-18
Regulation
880.5510
Classification name
Lift, Patient, Non-ac-powered
Medical specialty
General Hospital
Review panel
General Hospital
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FSA  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K942807SURGICAL LIFT SHEETSurgin Surgical Instrumentation, Inc.1994-08-02
K930625SANITAS PATIENT LIFTDutton-Lainson Co.1993-09-13
K902141ANOLIFT - PORTABLE & ANOLIFT - GANTRYAnodyne Corp.1990-09-12
K860837HOYER ONE-TOUCH POWER LIFTERTed Hoyer & Co., Inc.1986-03-27
K851844MOLIFTMadshus A/S1985-05-17
K844976MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFTMedi-Man Rehabilitation Products, Inc.1985-04-01
K841395SHOWER TROLLEYSetma, Inc.1984-05-07
K841398VARIABLE HEIGHT TRANSFER CHAIRSetma, Inc.1984-05-07
K840997BATTERY POWERED PATIENT LIFTInvacare Corp.1984-04-17
K823206MARTIN PELVIC LIFTMartin Pelvic Lift Co.1983-04-28
K811899CENTURY LIFT TRANSFER SYSTEMCentury Manufacturing Co.1981-07-23
K780684PATIENT LIFTOrthopedic Equipment Co., Inc.1978-06-06

Legacy Summary#

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FDA Review#

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