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

A-SCAN 100

K Number: K024114 · Decision Jan 10, 2003
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
9
Review Days
28

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Basic Information

Device Name
A-SCAN 100
K Number
K024114
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ophthalmic Technologies, Inc.
Date Received
December 13, 2002
Decision Date
January 10, 2003
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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