FDA 510(k) Substantially Equivalent 🇺🇸 United States

CANON AUTO REF KERATOMETER RK-1

K Number: K861415 · Decision May 14, 1986
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
48
Review Days
29

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Basic Information

Device Name
CANON AUTO REF KERATOMETER RK-1
K Number
K861415
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Canon USA, Inc.
Date Received
April 15, 1986
Decision Date
May 14, 1986
Advisory Committee
Unknown
Review Advisory Committee
OP
Third Party
N

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