Data / Medical devices / United States / Emerald Supply
Emerald Supply: FDA-registered device maker in Brooklyn, NY, United States, 1 510(k) clearance
Emerald Supply is registered with the FDA (registration 3011714211) in Brooklyn, NY, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 5, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011714211
- Address
- 1558 E 37th St, Brooklyn, NY, United States, 11234
- Owner or operator
- Emerald Supply (10051635)
- Roles
- Specification developer
- First device listed
- September 9, 2022
- Registered through
- 2026
- Brand names listed
- Selectis Serenity Elite, Semi Electric Bed
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Specification developer | accessdata.fda.gov |
| Mattress, Air Flotation, Alternating Pressure | FNM | 2 | Specification developer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| October 5, 2005 | K052468 | YK9000 SERIES MANUAL WHEELCHAIR | IOR | Substantially Equivalent | Intco Metal Products (Zhenjiang) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mattress, Air Flotation, Alternating Pressure
- All makers of Bed, Ac-Powered Adjustable Hospital
- All makers of Wheelchair, Mechanical
Updated October 5, 2005. 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.