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FDA 510(k)

DUAL TRACE VIDEO MONITOR VM 410

K-Number: K810165 · 1981-02-25

ApplicantHoneywell, Inc.
Decision Date1981-02-25
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DUAL TRACE VIDEO MONITOR VM 410 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810165. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL TRACE VIDEO MONITOR VM 410?

DUAL TRACE VIDEO MONITOR VM 410 is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Honeywell, Inc.. The 510(k) number is K810165.

When did DUAL TRACE VIDEO MONITOR VM 410 receive FDA 510(k) clearance?

DUAL TRACE VIDEO MONITOR VM 410 received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810165.

Who is the listed applicant for DUAL TRACE VIDEO MONITOR VM 410?

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

What is the FDA product code for DUAL TRACE VIDEO MONITOR VM 410?

The FDA product code for DUAL TRACE VIDEO MONITOR VM 410 is DXJ.

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Related Devices (Code: DXJ)

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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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