FDA 510(k)

TRANSDUCER

K-Number: K800093 · 1980-02-11

Decision Date1980-02-11

Product Code

DecisionSubstantially Equivalent

Device Summary

TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Kt Medical, Inc.. It received FDA 510(k) clearance on 1980-02-11 under 510(k) number K800093. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSDUCER?

TRANSDUCER is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Kt Medical, Inc.. The 510(k) number is K800093.

When did TRANSDUCER receive FDA 510(k) clearance?

TRANSDUCER received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800093.

Who is the listed applicant for TRANSDUCER?

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

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Other records listing Kt Medical, Inc. as applicant

K800653SINVISION LINEAR ARRAY REAL TIME K800652MODEL E03 ECHO-OPTHALMOSCOPE K8001014200 ME ECHOENCEPHALOGRAPH K800092COMBISON COMPUTER K800099INTRACULA II K8001007200 MA ECHO-OPHTHALMOSCOPE

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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.