D.R.O. Medical, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “D.R.O. Medical, Inc.” (first 1980, latest 1985), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 13 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
FPASet, Administration, Intravascular44
FMGStopcock, I.V. Set11

Review panels

Most recent D.R.O. Medical, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K844820FLOW MED SK 140 BURETFPA1985-01-2852
K820165FLOW MED 311FMG1982-02-0112
K801821FLOW MED 150FPA1980-08-1313
K801179FLOW MED 160FPA1980-05-3014
K801004FLOW MED 160FPA1980-05-027

Recalls

openFDA lists no recalls under a recalling firm named D.R.O. 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 D.R.O. Medical, Inc.?

FDA lists 5 510(k) clearances under the applicant name “D.R.O. Medical, Inc.” (first 1980, latest 1985), 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 D.R.O. Medical, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name D.R.O. Medical, Inc. is 13 days.

Which FDA product codes appear under D.R.O. Medical, Inc.?

The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 4); FMG (Stopcock, I.V. Set, 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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