Data / Medical devices / Hong Kong / LCCS Products Limited
LCCS Products Limited: FDA-registered device maker in Sai Ying Pun, Hong Kong, 5 510(k) clearances
LCCS Products Limited is registered with the FDA (registration 3009241989) in Sai Ying Pun, Hong Kong. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated January 24, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009241989
- Address
- Office 3a-7, 12/F, Kaiser Center, No. 18 Center Street, Sai Ying Pun, Hong Kong, NA
- Owner or operator
- LCCS Products Limited (10038005)
- Roles
- Specification developer
- First device listed
- September 6, 2011
- Registered through
- 2026
- Brand names listed
- ANESTHESIA CONDUCTION NEEDLES(Spinal Needle & Epidural Needle), Grounding Pad Adapt Cable, RF Cannula, RF Electrode, RF Electrode adapt Cable, Single Use Grounding Pad, VC-S RF Cannula
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable | ISN | 1 | Specification developer | accessdata.fda.gov |
| Cable, Electrode | IKD | 2 | Specification developer | accessdata.fda.gov |
| Electrode, Electrosurgical | JOS | 2 | Specification developer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Specification developer | accessdata.fda.gov |
| Needle, Conduction, Anesthetic (W/Wo Introducer) | BSP | 2 | Specification developer | accessdata.fda.gov |
| Probe, Radiofrequency Lesion | GXI | 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 |
|---|---|---|---|---|---|---|
| January 24, 2020 | K191293 | LCCS VC-S RF Cannula | GXI | Substantially Equivalent | Lccs Products Limited | accessdata.fda.gov |
| August 26, 2016 | K152642 | LCCS Disposable RF Electrode, LCCS Reusable RF Electrode | GXI | Substantially Equivalent | Lccs Products Limited | accessdata.fda.gov |
| December 6, 2013 | K131006 | ANESTHESIA CONDUCTION NEEDLES | BSP | Substantially Equivalent | Lccs Products Limited | accessdata.fda.gov |
| September 6, 2013 | K132136 | SINGLE USE GROUNDING PAD | GEI | Substantially Equivalent | Lccs Products Limited | accessdata.fda.gov |
| August 19, 2011 | K112231 | LCCS INSULATED SPINAL NEEDLE (RF CANNULA) | GXI | Substantially Equivalent | Lccs Products Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Cable, Electrode
- All makers of Probe, Radiofrequency Lesion
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Electrode, Electrosurgical
- All makers of Needle, Conduction, Anesthetic (W/Wo Introducer)
- All makers of Cable
Updated January 24, 2020. 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.