FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

YOSHIDA AP 100

K Number: K811211 · Decision Jun 16, 1981
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
8
Applicant Total
7
Review Days
43

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Basic Information

Device Name
YOSHIDA AP 100
K Number
K811211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1900
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Kaycor Intl., Ltd.
Date Received
May 4, 1981
Decision Date
June 16, 1981
Product Code
EGY
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EGY Processor, Radiographic-Film, Automatic, Dental

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Other Clearances by Kaycor Intl., Ltd.

K Number Device Name
K965072 PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT
K931717 YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY
K832063 ROBIN CORDLESS HANDPIECE
K822740 K30000 DENTAL CHAIR
K813348 YOSHIDA RIDO-F, MODEL LM-01
K811210 YOSHIDA-PANOURA 10