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

SONOMED 4000P ULTRASONIC PACHYMETER

K Number: K924311 · Decision Dec 8, 1992
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
8
Review Days
104

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Basic Information

Device Name
SONOMED 4000P ULTRASONIC PACHYMETER
K Number
K924311
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sonomed, Inc.
Date Received
August 26, 1992
Decision Date
December 8, 1992
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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K073196 MASTER-VU
K060626 VUMAX
K040668 E-Z SCAN AB5500+