Data / Medical devices / United States / Mcguff Company, Inc.
Mcguff Company, Inc.: FDA-registered device maker in Santa Ana, CA, United States, 1 510(k) clearance
Mcguff Company, Inc. is registered with the FDA (registration 3003189845) in Santa Ana, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 14, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003189845
- Address
- 3524 West Lake Center DRive, Santa Ana, CA, United States, 92704
- Owner or operator
- McGuff Company, Inc. (10076902)
- Roles
- Specification developer
- First device listed
- January 5, 2026
- Registered through
- 2026
- Brand names listed
- American Therapeutics Filtered IV Administration Set
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Set, Administration, Intravascular | FPA | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| August 14, 2021 | K210381 | I.V. Administration Set | FPA | Substantially Equivalent | Bq Plus Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 14, 2021. 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.