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