Data / Medical devices / United States / Radiation Products Design, Inc.

Radiation Products Design, Inc.: FDA-registered device maker in Albertville, MN, United States, 1 510(k) clearance

Name: Radiation Products Design, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Radiation Products Design, Inc. is registered with the FDA (registration 2182762) in Albertville, MN, United States. It lists 22 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 16, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 2182762
Address: 5218 Barthel Industrial Dr Ne, Albertville, MN, United States, 55301
Owner or operator: RADIATION PRODUCTS DESIGN, INC. (2182762)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: April 4, 1979
Registered through: 2026
Brand names listed: 3M Delclos Uterine/Vaginal Applicator W/O Tandems, 6cm Afterloading Barrel (S.S.) w/ Cap, Acrylic Cylinder w/ Suture Ring, Acrylic Cylinder w/ Suture Ring - 19mm Dia. X 120mm, Adjustable Point-to-Point Level, Adjustable Shielding Table w/ Wheels, Adult Chin Support w/Angle Indicator, Allen Wrench and more

Devices it lists

Device	Product code	Class	Role	Source
Accelerator, Linear, Medical	IYE	2	Manufacturer	accessdata.fda.gov
Bed, Manual	FNJ	1	Manufacturer	accessdata.fda.gov
Caliper	KTZ	1	Manufacturer	accessdata.fda.gov
Device, Transfer, Patient, Manual	FMR	1	Manufacturer	accessdata.fda.gov
Dispenser, Mercury And/Or Alloy	EHE	1	Manufacturer	accessdata.fda.gov
Holder, Head, Radiographic	IWY	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Holder, Syringe, Lead	IWR	1	Manufacturer	accessdata.fda.gov
Instrument, Quality-Assurance, Radiologic	LHO	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Lift, Patient, Non-Ac-Powered	FSA	1	Manufacturer	accessdata.fda.gov
Phantom, Anthropomorphic, Nuclear	IYP	1	Repackager or relabeler	accessdata.fda.gov
Protractor	HTH	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Shield, Eye, Radiological	IWS	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Shield, Gonadal	IWT	1	Manufacturer	accessdata.fda.gov
Shield, Protective, Personnel	KPY	1	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Stains, Dye Solution	LEE	1	Manufacturer	accessdata.fda.gov
Stand, Infusion	FOX	1	Manufacturer	accessdata.fda.gov
Support, Patient Position	CCX	1	Manufacturer	accessdata.fda.gov
System, Applicator, Radionuclide, Manual	IWJ	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
System, X-Ray, Film Marking, Radiographic	JAC	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Table, Powered	INQ	1	Manufacturer	accessdata.fda.gov
Table, Radiographic, Stationary Top	IXQ	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Test-Pattern, Radiographic	IXF	1	Manufacturer, Repackager or relabeler	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
September 16, 2015	K150382	Radio Therapy Treatment Chair	IYE	Substantially Equivalent	Radiation Products Design, Inc.	accessdata.fda.gov

Compare with other makers

Updated September 16, 2015. 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.