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510(k) K800373

Device
TENDERLIFT
Applicant
COMPETENT DESIGN
510(k) number
K800373
Product code
FMR  
Decision
Substantially Equivalent (SESE)
Decision date
1980-03-12
Date received
1980-02-20
Regulation
880.6785
Classification name
Device, Transfer, Patient, Manual
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 FMR  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K871475SOLOLIFT - PATIENT TRANSFER STRETCHERAdel Medical , Ltd.1987-05-11
K801796THE COMFORT LIFTGettner Enterprises, Inc.1980-08-13
K792318SKIL-CARE TURN AND HOLD PADSkil-Care Corp.1979-12-20
K770499PATIENT TURNING AND REPOSITIONING G DEV.Patient Healthguards Corp.1977-04-29

Legacy Summary#

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FDA Review#

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