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510(k) K828325

YOSHIDA/KAYCOR X-70 X-RAY UNIT by The Yoshida Dental Mfg. Co., Ltd.

K828325 is an FDA 510(k) premarket notification submitted by The Yoshida Dental Mfg. Co., Ltd. for the device "YOSHIDA/KAYCOR X-70 X-RAY UNIT". The FDA issued a decision of Substantially Equivalent on Oct 21, 1982. The Yoshida Dental Mfg. Co., Ltd. has 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Oct 21, 1982
Date Received
Sep 28, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by The Yoshida Dental Mfg. Co., Ltd.

  • K182198 — Panoura X-ERA PF/NF/MF (Jan 31, 2019)
  • K122199 — PREXION3D ECLIPSE (Apr 18, 2013)
  • K120948 — PREXION 3D (Dec 21, 2012)
  • K120932 — OPELASER PRO II AND THE OPELASER LITE II (Dec 7, 2012)
  • K111231 — PANOURA 18S (Jul 13, 2011)
  • K063622 — FINECUBE DENTAL CT (Feb 8, 2007)
  • K000577 — YOSHIDA WAVE PICT CAM INTRAORAL CAMERA, SIGMA BIOMEDICS SIGMACAM INTRAORAL… (May 5, 2000)
  • K837491 — REX PEDESTAL INTRA-ORAL X-RAY UNIT (Jun 13, 1983)

FDA data resources