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FDA 510(k)

VC 430 VIDEO CONVERTER

K-Number: K810164 · 1981-02-25

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

Device Summary

VC 430 VIDEO CONVERTER 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 K810164. 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 VC 430 VIDEO CONVERTER?

VC 430 VIDEO CONVERTER 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 K810164.

When did VC 430 VIDEO CONVERTER receive FDA 510(k) clearance?

VC 430 VIDEO CONVERTER received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810164.

Who is the listed applicant for VC 430 VIDEO CONVERTER?

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 VC 430 VIDEO CONVERTER?

The FDA product code for VC 430 VIDEO CONVERTER is 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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