Data / Medical devices / Hong Kong / RRC Power Solutions Ltd.
RRC Power Solutions Ltd.: FDA-registered device maker in Fo Tan, N.T., Hong Kong, 1 510(k) clearance
RRC Power Solutions Ltd. is registered with the FDA (registration 3013826848) in Fo Tan, N.T., Hong Kong. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2014. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013826848
- Address
- S-V,6/F, Valiant Industrial Centre 2-12 Au Pui Wan Street, Fo Tan, N.T., Hong Kong, 98052
- Owner or operator
- RRC power solutions Ltd. (10057892)
- Roles
- Exporter to the US
- First device listed
- June 9, 2018
- Registered through
- 2026
- Brand names listed
- AC TO DC POWER ADAPTER, LIFEPAK 15, ADAPTER - REDI-CHARGE BATTERY CHARGER, LIFEPAK 12, ADAPTER - REDI-CHARGE BATTERY CHARGER, LIFEPAK 15, BASE, REDI-CHARGE BATTERY CHARGER, CABLE - DC INPUT, DC POWER ADAPTER, DC TO DC POWER ADAPTER, LIFEPAK 15
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Exporter to the US | accessdata.fda.gov |
| Automated External Defibrillators (Non-Wearable) | MKJ | 3 | Exporter to the US | accessdata.fda.gov |
| Computer, Blood-Pressure | DSK | 2 | Exporter to the US | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Exporter to the US | accessdata.fda.gov |
| Dc-Defibrillator, Low-Energy, (Including Paddles) | LDD | 2 | Exporter to the US | accessdata.fda.gov |
| Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | DRT | 2 | Exporter to the US | accessdata.fda.gov |
| Oximeter | DQA | 2 | Exporter to the US | accessdata.fda.gov |
| Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) | DRO | 2 | Exporter to the US | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| December 19, 2014 | K142430 | LIFEPAK 15 monitor/defibrillator | MKJ | Substantially Equivalent | Physio-Control, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Computer, Blood-Pressure
- All makers of Oximeter
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- All makers of Dc-Defibrillator, Low-Energy, (Including Paddles)
Updated December 19, 2014. 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.