Cytocolor, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Cytocolor, Inc.” (first 1986, latest 1986), across 1 product code in 1 review panel. Median 510(k) review time under this name: 23 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
LEDStains, Chemical Solution55

Review panels

Most recent Cytocolor, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K860321LYSOCOLORLED1986-02-2023
K860320GRANULOCOLORLED1986-02-2023
K860319MEGACOLORLED1986-02-2023
K860317NEUTROCOLORLED1986-02-2023
K860316PANOPTIKONLED1986-02-2023

Recalls

openFDA lists no recalls under a recalling firm named Cytocolor, Inc..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Cytocolor, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Cytocolor, Inc.” (first 1986, latest 1986), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Cytocolor, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Cytocolor, Inc. is 23 days.

Which FDA product codes appear under Cytocolor, Inc.?

The most frequent FDA product codes under this applicant name are LED (Stains, Chemical Solution, 5).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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