Skip to the page

Data / Medical devices / United States / Nelson Environmental Technologies, Inc.

Nelson Environmental Technologies, Inc.: FDA-registered device maker in Arlington, TX, United States, 1 510(k) clearance

Nelson Environmental Technologies, Inc. is registered with the FDA (registration 3010867648) in Arlington, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 25, 2000. 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
3010867648
Address
1312 Corporate Dr. E Suite F, Arlington, TX, United States, 76006
Owner or operator
NELSON ENVIRONMENTAL TECHNOLOGIES, INC. (9039629)
Roles
Manufacturer
First device listed
December 14, 2007
Registered through
2026
Brand names listed
Nelson Water Systems for Hemodialys

Devices it lists

DeviceProduct codeClassRoleSource
Subsystem, Water PurificationFIP2Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 25, 2000K993877NELSON WATER SYSTEMS FOR HEMODIALYSISFIPSubstantially EquivalentNelson Environmental Technologies, Inc.accessdata.fda.gov

Compare with other makers

Updated May 25, 2000. 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.