ClearanceBrief
Company ยท US

Black & Decker(Tm)

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1982. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KIJInstrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment5
GEYMotor, Surgical Instrument, Ac-Powered2
HBCMotor, Drill, Electric1
LGHInstrument, Cast Removal, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 2, 1982K820351CAST CUTTER/CAST SAW/INSTRUMENT
Black & Decker(Tm)
LGH
Nov 2, 1981K812440POWER PACK
Black & Decker(Tm)
Nov 2, 1981K812439DUAL MPC CHARGER
Black & Decker(Tm)
Nov 2, 1981K812438SAGITTAL SAW
Black & Decker(Tm)
GEY
Nov 2, 1981K812437150 DRIVER REAMER
Black & Decker(Tm)
GEY
Nov 2, 1981K812436450/800 DRILL
Black & Decker(Tm)
HBC
Mar 19, 1980K800315DUAL MPC CHARGER
Black & Decker(Tm)
KIJ
Mar 19, 1980K800314POWER PACK
Black & Decker(Tm)
KIJ
Feb 22, 1980K800313SAGITTAL SAW
Black & Decker(Tm)
KIJ
Feb 22, 1980K800312150 DRIVER/REAMER
Black & Decker(Tm)
KIJ
Feb 22, 1980K800311450 DRILL/800 DRILL
Black & Decker(Tm)
KIJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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