Siemens Medical Corp.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Siemens Medical Corp.” (first 1999, latest 2001), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 72 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
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Top product codes

Product codeDeviceSubmissions510(k) clearances
LNHSystem, Nuclear Magnetic Resonance Imaging22
IZISystem, X-Ray, Angiographic11
JAKSystem, X-Ray, Tomography, Computed11
ODAEndoscopic Central Control Unit11

Review panels

Most recent Siemens Medical Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K012202NUMARIS 4VA15ALNH2001-09-2776
K010721AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEMIZI2001-03-3018
K994231SIEMENS INTEGRATED OPERATING SYSTEM (SIOS)ODA2000-08-10238
K994316MAGNETOM OPEN VIVA WITH PERMANENT MAGNETLNH2000-01-1423
K9846343D-ANGIOJAK1999-03-1272

Recalls

openFDA lists no recalls under a recalling firm named Siemens Medical Corp..

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.

Related HCPCS codes

HCPCS Level II codes whose descriptors match the device names of the product codes filed under Siemens Medical Corp. (a text match, not an official crosswalk):

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 Corp.?

FDA lists 5 510(k) clearances under the applicant name “Siemens Medical Corp.” (first 1999, latest 2001), across 4 product codes in 2 review panels. 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 Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Siemens Medical Corp. is 72 days.

Which FDA product codes appear under Siemens Medical Corp.?

The most frequent FDA product codes under this applicant name are LNH (System, Nuclear Magnetic Resonance Imaging, 2); IZI (System, X-Ray, Angiographic, 1); 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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