FDA 510(k)

Kent Camera

K-Number: K163070 · 2017-05-05

Decision Date2017-05-05

Product CodeMUD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Kent Camera is the device name listed in this FDA 510(k) record. The listed applicant is Kent Imaging, Inc.. It received FDA 510(k) clearance on 2017-05-05 under 510(k) number K163070. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kent Camera?

Kent Camera is a medical device that received FDA 510(k) clearance on 2017-05-05. The listed applicant is Kent Imaging, Inc.. The 510(k) number is K163070.

When did Kent Camera receive FDA 510(k) clearance?

Kent Camera received FDA 510(k) clearance on 2017-05-05, under 510(k) number K163070.

Who is the listed applicant for Kent Camera?

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

What is the FDA product code for Kent Camera?

The FDA product code for Kent Camera is MUD.

Other records listing Kent Imaging, 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.