Bmw Medical, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Bmw Medical, Inc.” (first 1996, latest 1997), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 84 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
LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days44
FPASet, Administration, Intravascular11

Review panels

Most recent Bmw Medical, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K964439NEEDLE-FREE VALVED CONNECTOR AND CAPFPA1997-07-16252
K963806CLAMPLESS VALVED CATHETER - TUNNELED (CVC-T)LJS1996-12-1280
K963215CLAMPLESS VALVED CATHETER - MIDLINE (CVC-ML)LJS1996-11-1490
K963097CLAMPLESS VALVED CATHETER-PICC (CVC-PICC)LJS1996-10-1870
K962300CLAMPLESS VALVED CATHETERLJS1996-09-0584

Recalls

openFDA lists no recalls under a recalling firm named Bmw Medical, 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 Bmw Medical, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Bmw Medical, Inc.” (first 1996, latest 1997), 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 Bmw Medical, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Bmw Medical, Inc. is 84 days.

Which FDA product codes appear under Bmw Medical, Inc.?

The most frequent FDA product codes under this applicant name are LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days, 4); FPA (Set, Administration, Intravascular, 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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