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

OPHTHALMIC A-SCAN A-2000 SONOME

K Number: K843696 · Decision Feb 26, 1985
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
5
Review Days
160

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Basic Information

Device Name
OPHTHALMIC A-SCAN A-2000 SONOME
K Number
K843696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Sonomed Technology, Inc.
Date Received
September 19, 1984
Decision Date
February 26, 1985
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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Other Clearances by Sonomed Technology, Inc.

K Number Device Name
K931908 SONOQUICK ULTRASOUND GEL
K931909 CLEAR IMAGE STERILE DIAGNOSTIC ULTRSOUND GEL
K883917 NATURAL IMAGE ULTRASOUND TRANSMISSION COUPLANT
K844031 SONOMED TECH OPHTHALMIC B-SCAN B-3000