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510(k) K910830

Device
INVALIFT
Applicant
AMERICAN INVALIFT CORP.
510(k) number
K910830
Product code
FRZ  
Decision
Substantially Equivalent (SESE)
Decision date
1992-06-09
Date received
1991-02-27
Regulation
880.6775
Classification name
Device, Patient Transfer, Powered
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
THERESE RUBINO
Address
285 Tarrytown Rd. White Plains NY US 10607 10607

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FRZ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K121929ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDDiacor, Inc.2013-01-17
K841728LCI MEDICAL INC AIR/PALLehigh Consolidated Industries1984-06-05
K834585CELLTRAK-BR&D Systems, Inc.1984-05-02
K840796TENDER LIFTING CARELancer Assoc.1984-04-20

Legacy Summary#

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FDA Review#

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