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FDA 510(k)

TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER

K-Number: K883546 · 1988-10-07

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1988-10-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K883546. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER?

TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K883546.

When did TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER receive FDA 510(k) clearance?

TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER received FDA 510(k) clearance on 1988-10-07, under 510(k) number K883546.

Who is the listed applicant for TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER?

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

What is the FDA product code for TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER?

The FDA product code for TEEC (TRANSESOPHAGEAL ECHOCARDIOGRAPHY) TRANSDUCER is IYO.

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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.

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