Data / Medical devices / Amplifier And Signal Conditioner, Transducer Signal / United States
FDA-registered makers of Amplifier And Signal Conditioner, Transducer Signal in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Amplifier And Signal Conditioner, Transducer Signal (product code DRQ). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Amplifier And Signal Conditioner, Transducer Signal
- Product code
- DRQ
- Country
- United States
Makers of Amplifier And Signal Conditioner, Transducer Signal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Boston Scientific Corporation | Saint Paul, MN, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | October 21, 2015 | 0 | 0 | 0 | api.fda.gov |
| Acist Medical Systems, Inc. | Eden Prairie, MN, United States | Manufacturer, Manufacturer for export | 1 | August 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| Draeger Medical Systems, Inc. | Andover, MA, United States | Manufacturer | 1 | April 29, 2005 | 0 | 0 | 0 | api.fda.gov |
| Millar LLC. | Houston, TX, United States | Manufacturer | 1 | July 2, 2002 | 0 | 0 | 0 | api.fda.gov |
| MINDRAY DS USA, Inc. | Mahwah, NJ, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Multisource MFG. LLC | Fridley, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden Digital Health Solutions, LLC. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Cambridge, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Andover, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Murrysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Export, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phillips-Medisize Costa Mesa LLC | Costa Mesa, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.