510(k) K800373

TENDERLIFT by Competent Design — Product Code FMR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 12, 1980
Date Received
February 20, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Transfer, Patient, Manual
Device Class
Class I
Regulation Number
880.6785
Review Panel
HO
Submission Type