Data / Medical devices / United States / Midmark Corp.
Midmark Corp.: FDA-registered device maker in Blue Ash, OH, United States, 1 510(k) clearance
Midmark Corp. is registered with the FDA (registration 3043668257) in Blue Ash, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 22, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043668257
- Address
- 9987 Carver Rd Ste 310, Blue Ash, OH, United States, 45242
- Owner or operator
- MIDMARK CORP. (9915004)
- Roles
- Specification developer
- First device listed
- December 14, 2016
- Registered through
- 2026
- Brand names listed
- Midmark IQecg Electrocardiograph
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrocardiograph | DPS | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 22, 2011 | K103640 | MIDMARK IQECG | DPS | Substantially Equivalent | Brentwood Medical Technology Corp. | accessdata.fda.gov |
Compare with other makers
Updated March 22, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.