Cleared Traditional

K891238 - SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER

K891238 is an FDA 510(k) clearance for SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER, manufactured by Siemens Ultrasound, Inc.. The device is a Class 2 Radiology device with product code IYN cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K891238 · Siemens Ultrasound, Inc. · Radiology device
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Jun 1989
Decision
90d
Days
Class 2
Risk

K891238 is an FDA 510(k) clearance for the SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER. Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by Siemens Ultrasound, Inc. (Pleasanton, US). The FDA issued a Cleared decision on June 5, 1989 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - 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 Siemens Ultrasound, Inc. devices

FDA 510(k) Submission Details - K891238

510(k) Number K891238 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 1989
Decision Date June 05, 1989
Days to Decision 90 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 107d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYN Device Classification - Class 2, Special Controls

Product Code IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1550
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 - IYN System, Imaging, Pulsed Doppler, Ultrasonic

All 1143
Devices cleared under the same product code (IYN) and FDA review panel - the closest regulatory comparables to K891238.
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