Data / Medical devices / United Kingdom / Prestige Medical, Ltd.
Prestige Medical, Ltd.: FDA-registered device maker in BLACKBURN Lancashire, United Kingdom, 1 510(k) clearance
Prestige Medical, Ltd. is registered with the FDA (registration 3008342949) in BLACKBURN Lancashire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 3, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008342949
- Address
- East House, Duttons Way, Shadsworth Business Park, BLACKBURN Lancashire, United Kingdom, BB1 2QR
- Owner or operator
- PRESTIGE MEDICAL, LTD. (9019717)
- Roles
- Manufacturer
- First device listed
- December 5, 2007
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sterilizer, Steam | FLE | 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 |
|---|---|---|---|---|---|---|
| March 3, 1998 | K962903 | PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE | FLE | Substantially Equivalent | Prestige Medical Corp. | accessdata.fda.gov |
Compare with other makers
Updated March 3, 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.