Algotec Systems, Ltd.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Algotec Systems, Ltd.” (first 1996, latest 2003), across 1 product code in 1 review panel. Median 510(k) review time under this name: 78 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

Review panels

Most recent Algotec Systems, Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K033013MDIFICATION TO MEDIPRIMELLZ2003-11-2560
K023936MODIFICATION TO MEDIPRIMELLZ2002-12-2024
K002894MEDIPRIMELLZ2000-12-0578
K980648PRO VISIONLLZ1998-07-20151
K954678PRO VISIONLLZ1996-01-0587

Recalls

openFDA lists no recalls under a recalling firm named Algotec Systems, Ltd..

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 Algotec Systems, Ltd.?

FDA lists 5 510(k) clearances under the applicant name “Algotec Systems, Ltd.” (first 1996, latest 2003), 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 Algotec Systems, Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Algotec Systems, Ltd. is 78 days.

Which FDA product codes appear under Algotec Systems, Ltd.?

The most frequent FDA product codes under this applicant name are LLZ (System, Image Processing, Radiological, 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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