Siemens Medical Solutions USA, Inc., Ultrasound DI: FDA filings under this applicant name

FDA lists 11 510(k) clearances under the applicant name “Siemens Medical Solutions USA, Inc., Ultrasound DI” (first 2007, latest 2017), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 44 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

Caduvo groups this applicant name under Siemens Healthineers, based on public ownership records.

510(k) clearances per year

YearClearancesMedian review days
20120—
20130—
20140—
20150—
20160—
2017179
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Siemens Medical Solutions USA, Inc., Ultrasound DI took a median 79 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 109 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
IYNSystem, Imaging, Pulsed Doppler, Ultrasonic88
IYOSystem, Imaging, Pulsed Echo, Ultrasonic22
JAKSystem, X-Ray, Tomography, Computed11

Review panels

Most recent Siemens Medical Solutions USA, Inc., Ultrasound DI 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K163289syngo. CT Single Source Dual Energy (twin beam)JAK2017-02-0979
K113179ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEMIYN2011-12-0740
K112596ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEMIYN2011-09-169
K081148SIEMENS ACUSON 2000 ULTRASOUND SYSTEM WITH ABVS TRANSDUCERIYO2008-12-22244
K082142ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEMIYN2008-11-13106
K081121MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEMIYO2008-06-0444
K080760ACUSON X300 ULTRASOUND SYSTEMIYN2008-04-2538
K072365SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEMIYN2007-10-1755
K072090SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMSIYN2007-09-1446
K071036MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEMIYN2007-05-1634

1 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Siemens Medical Solutions USA, Inc., Ultrasound DI.

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.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Siemens Medical Solutions USA, Inc., Ultrasound DI?

FDA lists 11 510(k) clearances under the applicant name “Siemens Medical Solutions USA, Inc., Ultrasound DI” (first 2007, latest 2017), across 3 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 Siemens Medical Solutions USA, Inc., Ultrasound DI?

The median time from FDA receipt to decision across 510(k)s cleared under the name Siemens Medical Solutions USA, Inc., Ultrasound DI is 44 days.

Which FDA product codes appear under Siemens Medical Solutions USA, Inc., Ultrasound DI?

The most frequent FDA product codes under this applicant name are IYN (System, Imaging, Pulsed Doppler, Ultrasonic, 8); IYO (System, Imaging, Pulsed Echo, Ultrasonic, 2); JAK (System, X-Ray, Tomography, Computed, 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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