The Master Medical Corp.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “The Master Medical Corp.” (first 1979, latest 1991), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 114 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
LDRController, Infusion, Intravascular, Electronic22

Review panels

Most recent The Master Medical Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K913076I.V. INSTANT TIMERFPA1991-10-1798
K905498STAT 2 IV PUMPETTELDR1991-04-16130
K905497MASTER FLOW I.V. PUMPETTELDR1991-04-16130
K871753MASTER MEDICAL DEVICE IS I.V. STAT 2FPA1987-06-0531
K852254I.V. STAT MASTERFPA1985-11-18178
K792560MASTER I.V. DIAL LOCKFPA1979-12-209

Recalls

openFDA lists no recalls under a recalling firm named The Master 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.

Frequently asked questions

How many FDA 510(k) clearances are listed under The Master Medical Corp.?

FDA lists 6 510(k) clearances under the applicant name “The Master Medical Corp.” (first 1979, latest 1991), 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 The Master Medical Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name The Master Medical Corp. is 114 days.

Which FDA product codes appear under The Master Medical Corp.?

The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 4); LDR (Controller, Infusion, Intravascular, Electronic, 2).

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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