FDA 510(k)

SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER

K-Number: K891238 · 1989-06-05

Decision Date1989-06-05

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Ultrasound, Inc.. It received FDA 510(k) clearance on 1989-06-05 under 510(k) number K891238. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER?

SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is Siemens Ultrasound, Inc.. The 510(k) number is K891238.

When did SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER receive FDA 510(k) clearance?

SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER received FDA 510(k) clearance on 1989-06-05, under 510(k) number K891238.

Who is the listed applicant for SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER?

The FDA 510(k) record lists Siemens Ultrasound, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER?

The FDA product code for SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER is IYN.

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Other records listing Siemens Ultrasound, Inc. as applicant

K914013SIEMENS SI-400 K912361SI-450/ILUS (INTRALUMINAL ULTRASOUND)K911200SI-1200 / ILUS K904017SIEMENS SONOLINE SI-450, OB/GYN,ENT,DENTAL DEVICES K9105297.5 MHZ PEDIATRIC TRANSESOPHAGEAL ECHO (TEE) TRANS K9106695 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU

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Related Devices (Code: IYN)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.