Mid-Canada Medical: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Mid-Canada Medical” (first 1988, latest 1994), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 157 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
GZJStimulator, Nerve, Transcutaneous, For Pain Relief11
ILJBath, Hydro-Massage11
IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat11
INMChair, With Casters11
LIHInterferential Current Therapy11

Review panels

Most recent Mid-Canada Medical 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K933237MEDI-STIM, MODIFICATIONGZJ1994-09-08441
K922839MID-CANADA MEDICALIMI1993-07-02385
K921491MEDI-STIMLIH1992-09-03157
K883309MULTI-CARE CHAIRINM1988-09-3056
K883308PARKER BATHING SYSTEMILJ1988-09-2248

Recalls

openFDA lists no recalls under a recalling firm named Mid-Canada Medical.

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 Mid-Canada Medical?

FDA lists 5 510(k) clearances under the applicant name “Mid-Canada Medical” (first 1988, latest 1994), across 5 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 Mid-Canada Medical?

The median time from FDA receipt to decision across 510(k)s cleared under the name Mid-Canada Medical is 157 days.

Which FDA product codes appear under Mid-Canada Medical?

The most frequent FDA product codes under this applicant name are GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief, 1); ILJ (Bath, Hydro-Massage, 1); IMI (Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat, 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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