Data / Medical devices / United States / Stickman Dialysis Industries Inc.
Stickman Dialysis Industries Inc.: FDA-registered device maker in Arundel, ME, United States, 1 510(k) clearance
Stickman Dialysis Industries Inc. is registered with the FDA (registration 3012706378) in Arundel, ME, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 27, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012706378
- Address
- 39 Enterprise Drive, Arundel, ME, United States, 04046
- Owner or operator
- STICKMAN Dialysis Industries Inc. (9049807)
- Roles
- Manufacturer
- First device listed
- December 26, 2002
- Registered through
- 2026
- Brand names listed
- yeah whatever. I did this a thouisand times already for fuck's sake.
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Peritoneal | GBW | 1 | Manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Manufacturer | accessdata.fda.gov |
| Warmer, Peritoneal Dialysate | MLW | 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 |
|---|---|---|---|---|---|---|
| September 27, 2002 | K020542 | DAYTRIPPER DIALYSATE WARMER | MLW | Substantially Equivalent | Stickman Industries, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stand, Infusion
- All makers of Warmer, Peritoneal Dialysate
- All makers of Catheter, Peritoneal
Updated September 27, 2002. 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.