Data / Medical devices / United States / RGF Environmental Group, Inc
RGF Environmental Group, Inc: FDA-registered device maker in Riviera Beach, FL, United States, 2 510(k) clearances
RGF Environmental Group, Inc is registered with the FDA (registration 3014498814) in Riviera Beach, FL, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 23, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014498814
- Address
- 1101 W13th St., Riviera Beach, FL, United States, 33404
- Owner or operator
- RGF Environmental Group, Inc (10057519)
- Roles
- Manufacturer
- First device listed
- April 18, 2018
- Registered through
- 2026
- Brand names listed
- MICROCON 400M, MICROCON 400MUV, MICROCON 800M, MICROCON 800MUV, MICROCON EX, MICROCON EXC, MICROCON EXC-BUV, MICROCON WALLMAP
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cleaner, Air, Medical Recirculating | FRF | 2 | Manufacturer | accessdata.fda.gov |
| Purifier, Air, Ultraviolet, Medical | FRA | 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 |
|---|---|---|---|---|---|---|
| January 23, 1998 | K974682 | MICROCON 800M, MICROCON 400M, MICROCON EXC, MICROCON EX, MICROCON WALLMAP | FRF | Substantially Equivalent | Biological Controls, Inc. | accessdata.fda.gov |
| December 1, 1997 | K972064 | MICROCON 800MUV, MICROCON 400MUV, MICROCON EXC-BUV | FRA | Substantially Equivalent | Biological Controls, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 23, 1998. 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.