Cleared Traditional

K802438 - MARK V DUPLEX ULTRASONIC SCAN SYS.

K802438 is the FDA 510(k) clearance for MARK V DUPLEX ULTRASONIC SCAN SYS. by Advanced Technology Laboratories, Inc.. It is a Class 2 Radiology device (product code ITX) cleared through the Traditional 510(k) pathway after a 107-day FDA review.

K802438 · Advanced Technology Laboratories, Inc. · Radiology device
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Jan 1981
Decision
107d
Days
Class 2
Risk

K802438 is an FDA 510(k) clearance for the MARK V DUPLEX ULTRASONIC SCAN SYS.. Classified as Transducer, Ultrasonic, Diagnostic (product code ITX), Class II - Special Controls.

Submitted by Advanced Technology Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 21, 1981 after a review of 107 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1570 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Advanced Technology Laboratories, Inc. devices

Submission Details

510(k) Number K802438 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 06, 1980
Decision Date January 21, 1981
Days to Decision 107 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
At panel average
Panel avg: 107d · This submission: 107d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code ITX Transducer, Ultrasonic, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1570
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - ITX Transducer, Ultrasonic, Diagnostic

All 202
Devices cleared under the same product code (ITX) and FDA review panel - the closest regulatory comparables to K802438.
BIOPSY TRANSDUCER
K811843 · Siemens Gammasonics, Inc. · Aug 1981
7.5 MHZ WP TRANSDUCER
K810748 · General Electric Co. · Jun 1981
5 MHZ TRANSDUCER
K810749 · General Electric Co. · Apr 1981
IN-LINE SCAN HEAD MODIFICATION MARK III
K801971 · Advanced Technology Laboratories, Inc. · Oct 1980
IN-LINE SCAN HEAD MARK IV DUPLEX ULTRA
K801973 · Advanced Technology Laboratories, Inc. · Oct 1980