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

ATL'S MARK 100/300 ULTRASOUND SYSTEMS

K Number: K811572 · Decision Aug 10, 1981
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
61
Review Days
67

Basic Information

Device Name
ATL'S MARK 100/300 ULTRASOUND SYSTEMS
K Number
K811572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Date Received
June 4, 1981
Decision Date
August 10, 1981
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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