ClearanceBrief
Company ยท US

Kaycor Intl., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1997. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EKXHandpiece, Direct Drive, Ac-Powered2
EAPUnit, X-Ray, Intraoral1
EGYProcessor, Radiographic-Film, Automatic, Dental1
EHDUnit, X-Ray, Extraoral With Timer1
KLCChair, Dental, With Operative Unit1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 27, 1997K965072PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT
Kaycor Intl., Ltd.
EHD
Sep 20, 1993K931717YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY
Kaycor Intl., Ltd.
EAP
Aug 26, 1983K832063ROBIN CORDLESS HANDPIECE
Kaycor Intl., Ltd.
EKX
Sep 28, 1982K822740K30000 DENTAL CHAIR
Kaycor Intl., Ltd.
KLC
Jan 7, 1982K813348YOSHIDA RIDO-F, MODEL LM-01
Kaycor Intl., Ltd.
EKX
Aug 24, 1981K811210YOSHIDA-PANOURA 10
Kaycor Intl., Ltd.
Jun 16, 1981K811211YOSHIDA AP 100
Kaycor Intl., Ltd.
EGY

Latest recalls

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