Data / Medical devices / United States / Anybattery, Inc
Anybattery, Inc: FDA-registered device maker in Rosemount, MN, United States, 1 510(k) clearance
Anybattery, Inc is registered with the FDA (registration 3005521864) in Rosemount, MN, United States. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 11, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005521864
- Address
- 2605 160TH W Ste 116, Rosemount, MN, United States, 55068
- Owner or operator
- ANYBATTERY, INC (9074781)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- July 5, 2005
- Registered through
- 2026
- Brand names listed
- 1045, 1149, 1149-2, 2424-1, 2594, 3394, 3777, 4028 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Battery, Replacement, Rechargeable | MOQ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dc-Defibrillator, Low-Energy, (Including Paddles) | LDD | 2 | Manufacturer | accessdata.fda.gov |
| Electrocardiograph | DPS | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | DRT | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | MHX | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 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 |
|---|---|---|---|---|---|---|
| May 11, 2017 | K160667 | Anybattery C2 Rechargeable Battery | DPS | Substantially Equivalent | Anybattery, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrocardiograph
- All makers of Dc-Defibrillator, Low-Energy, (Including Paddles)
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- All makers of Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- All makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Updated May 11, 2017. 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.