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FDA 510(k)

CAMPBRIDGE COMPUTRACE

K-Number: K811062 · 1981-05-29

ApplicantCambridge Instruments, Inc.
Decision Date1981-05-29
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAMPBRIDGE COMPUTRACE is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Instruments, Inc.. It received FDA 510(k) clearance on 1981-05-29 under 510(k) number K811062. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPBRIDGE COMPUTRACE?

CAMPBRIDGE COMPUTRACE is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K811062.

When did CAMPBRIDGE COMPUTRACE receive FDA 510(k) clearance?

CAMPBRIDGE COMPUTRACE received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811062.

Who is the listed applicant for CAMPBRIDGE COMPUTRACE?

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

What is the FDA product code for CAMPBRIDGE COMPUTRACE?

The FDA product code for CAMPBRIDGE COMPUTRACE is DXG.

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Other records listing Cambridge Instruments, Inc. as applicant

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Related Devices (Code: DXG)

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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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