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DWH — Blade, Saw, Surgical, Cardiovascular Class I

FDA Device Classification

Classification Details

Product Code
DWH
Device Class
Class I
Regulation Number
878.4820
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K904352codman and shurtleffCODMAN COLLINS RADIOPARENT STERNAL BLADESNovember 21, 1990
K862474hall surgical, division of zimmerHALL STERNUM SAWJuly 17, 1986
K850483micro-aire surgical instrumentsMICRO-AIRE STERNUM SAW REPLACEMENT BLADESMarch 1, 1985
K830189temp medical productsCARDIOVASCULAR SAW BLADESMarch 24, 1983