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510(k) K811210

YOSHIDA-PANOURA 10 by Kaycor Intl., Ltd.

K811210 is an FDA 510(k) premarket notification submitted by Kaycor Intl., Ltd. for the device "YOSHIDA-PANOURA 10". The FDA issued a decision of Substantially Equivalent on August 24, 1981. Kaycor Intl., Ltd. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 24, 1981
Date Received
May 4, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Kaycor Intl., Ltd.

  • K965072 — PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT (January 27, 1997)
  • K931717 — YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY (September 20, 1993)
  • K832063 — ROBIN CORDLESS HANDPIECE (August 26, 1983)
  • K822740 — K30000 DENTAL CHAIR (September 28, 1982)
  • K813348 — YOSHIDA RIDO-F, MODEL LM-01 (January 7, 1982)
  • K811211 — YOSHIDA AP 100 (June 16, 1981)

FDA data resources