Data / Medical devices / United States / Micro Medical Solutions Inc
Micro Medical Solutions Inc: FDA-registered device maker in Woburn, MA, United States, 2 510(k) clearances
Micro Medical Solutions Inc is registered with the FDA (registration 3013391155) in Woburn, MA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 25, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013391155
- Address
- 175 New Boston St Ste H, Woburn, MA, United States, 01801
- Owner or operator
- Micro Medical Solutions Inc (10059633)
- Roles
- Manufacturer
- First device listed
- February 5, 2019
- Registered through
- 2026
- Brand names listed
- MicroBalloon, MicroGuide
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Angioplasty, Peripheral, Transluminal | LIT | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Continuous Flush | KRA | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 25, 2016 | K152934 | MMS PTA Balloon Catheter | LIT | Substantially Equivalent | Micro Medical Solutions, Inc. | accessdata.fda.gov |
| March 9, 2016 | K152625 | MMS Guide Catheter | KRA | Substantially Equivalent | Micro Medical Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Angioplasty, Peripheral, Transluminal
- All makers of Catheter, Continuous Flush
Updated April 25, 2016. 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.