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FDA 510(k)

TRACOR MODEL RA-411 MICROPROCESSOR

K-Number: K790903 · 1979-05-31

ApplicantTracor Instruments, Inc.
Decision Date1979-05-31
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TRACOR MODEL RA-411 MICROPROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Tracor Instruments, Inc.. It received FDA 510(k) clearance on 1979-05-31 under 510(k) number K790903. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACOR MODEL RA-411 MICROPROCESSOR?

TRACOR MODEL RA-411 MICROPROCESSOR is a medical device that received FDA 510(k) clearance on 1979-05-31. The listed applicant is Tracor Instruments, Inc.. The 510(k) number is K790903.

When did TRACOR MODEL RA-411 MICROPROCESSOR receive FDA 510(k) clearance?

TRACOR MODEL RA-411 MICROPROCESSOR received FDA 510(k) clearance on 1979-05-31, under 510(k) number K790903.

Who is the listed applicant for TRACOR MODEL RA-411 MICROPROCESSOR?

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

What is the FDA product code for TRACOR MODEL RA-411 MICROPROCESSOR?

The FDA product code for TRACOR MODEL RA-411 MICROPROCESSOR is EWO.

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Other records listing Tracor Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K853245TRACOR MODEL RA600 MICROPROCESSOR AUDIOMETERK851392TRACOR 200 MICROPROCESSOR AUDIOMETER/TRACOR RA 200K822414TRACOR RA400 AUDIOMETERK781743RESPONSE SYSTEM, TN-3000K781704STIMULATOR, TN-3001 SOMATOSENSORYK780749SPEECH AUDIOMETER RA 226

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Related Devices (Code: EWO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K234095OtoNova/OtoNova ProOtodynamicsK240430Otoport ProOtodynamics, Ltd.K231545hearOAEHearx SA (Pty) , Ltd.K213345Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONEPath Medical GmbHK191372LyraInteracoustics A/SK180287GSI CortiGrason-Stadler, Inc.

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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