FDA 510(k) Substantially Equivalent 🇨🇦 Canada

CORNEOMAP 4500 ULTRASOUND MEASUREMENT

K Number: K837331 · Decision May 9, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
5
Review Days
60

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Basic Information

Device Name
CORNEOMAP 4500 ULTRASOUND MEASUREMENT
K Number
K837331
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Radionics Medical, Inc.
Date Received
March 10, 1983
Decision Date
May 9, 1983
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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K844299 CORNEOMAP 4500
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K810851 SPECTRUM ANALYZER 8000