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KNL — Board, Scooter, Prone Class I

FDA Device Classification

Classification Details

Product Code
KNL
Device Class
Class I
Regulation Number
890.5370
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K841695maddakCRAWLERMay 10, 1984
K811489fred sammonsSCOOTER BOARDJune 12, 1981
K790528maddakTHERAPY GYROSCOPEApril 3, 1979
K781198fred sammonsBOARD, SCOOTERJuly 31, 1978
K780296convaid product developmentTHERAPY SCOOTERFebruary 24, 1978