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

POCKET ULTRASONIC OPHTHALMIC PACHYMETER, BIOMETRY TRANSDUCER FOR POCKET

K Number: K000554 · Decision Mar 14, 2000
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
30
Review Days
25

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Basic Information

Device Name
POCKET ULTRASONIC OPHTHALMIC PACHYMETER, BIOMETRY TRANSDUCER FOR POCKET
K Number
K000554
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quantel Medical
Date Received
February 18, 2000
Decision Date
March 14, 2000
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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