Segami Corporation: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Segami Corporation” (first 1997, latest 2007), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 51 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
LLZSystem, Image Processing, Radiological55
KPSSystem, Tomography, Computed, Emission11

Review panels

Most recent Segami Corporation 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K071584OASIS RELEASE 1.0LLZ2007-08-3181
K070397DGSCOPE, RELEASE 1.0LLZ2007-04-1360
K070683MIRAGE CEDARS OPTIONLLZ2007-04-1231
K043441MIRAGE, RELEASE 5.5KPS2005-01-1330
K010726MODIFICATION TO MIRAGELLZ2001-04-2645
K972886MIRAGELLZ1997-10-0157

Recalls

openFDA lists no recalls under a recalling firm named Segami Corporation.

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 Segami Corporation?

FDA lists 6 510(k) clearances under the applicant name “Segami Corporation” (first 1997, latest 2007), across 2 product codes 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 Segami Corporation?

The median time from FDA receipt to decision across 510(k)s cleared under the name Segami Corporation is 51 days.

Which FDA product codes appear under Segami Corporation?

The most frequent FDA product codes under this applicant name are LLZ (System, Image Processing, Radiological, 5); KPS (System, Tomography, Computed, Emission, 1).

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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