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FDA 510(k)

TRT TRANS-RECTAL TRANSDUCER

K-Number: K870038 · 1987-03-30

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1987-03-30
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRT TRANS-RECTAL 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 1987-03-30 under 510(k) number K870038. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRT TRANS-RECTAL TRANSDUCER?

TRT TRANS-RECTAL TRANSDUCER is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K870038.

When did TRT TRANS-RECTAL TRANSDUCER receive FDA 510(k) clearance?

TRT TRANS-RECTAL TRANSDUCER received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870038.

Who is the listed applicant for TRT TRANS-RECTAL 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 TRT TRANS-RECTAL TRANSDUCER?

The FDA product code for TRT TRANS-RECTAL TRANSDUCER is ITX.

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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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