Data / Medical devices / United States / MPS Pharma & Medical, Inc.
MPS Pharma & Medical, Inc.: FDA-registered device maker in Brea, CA, United States, 13 510(k) clearances
MPS Pharma & Medical, Inc. is registered with the FDA (registration 3018125942) in Brea, CA, United States. It lists 7 device types. The FDA files 13 510(k) clearances under its listings, the newest dated November 10, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018125942
- Address
- 465 N. Berry Street, Brea, CA, United States, 92821
- Owner or operator
- MPS Pharma & Medical, Inc. (10080968)
- Roles
- Manufacturer
- First device listed
- March 9, 2021
- Registered through
- 2026
- Brand names listed
- 1 Pharm-6, Single Lead High Volume Pump Chamber, 1 Pharm-6FG, Single Lead High Volume Pump Chamber Set, 17787HP3M, Triple Lead High Volume Pump Chamber Set, 17788HP3M, Dual Lead High Volume Pump Chamber Set, 17789HP, Single Lead High Volume Pump Chamber Set, 17789HP3M, Single Lead High Volume Pump Chamber Set, 17789HP3M-10PK, Single Lead High Volume Pump Chamber Set, 17789HP3MLL-10PK, Single Lead High Volume pump Chamber Set and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Media Dispensing/Stacking | JTB | 1 | Manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | accessdata.fda.gov |
| Set, I.V. Fluid Transfer | LHI | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
| System/Device, Pharmacy Compounding | NEP | 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 |
|---|---|---|---|---|---|---|
| November 10, 2010 | K103165 | BLOOD SAMPLING SET | FPA | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| April 28, 2009 | K090809 | MPS ACACIA POWER INJECTABLE INFUSION SET | FPA | Substantially Equivalent | Mps Acacia | accessdata.fda.gov |
| January 20, 1999 | K983926 | MPS GRAVITY FLOW CONTROL SET | FPA | Substantially Equivalent | Critical Device Corp. | accessdata.fda.gov |
| August 24, 1998 | K982587 | MPS FIXED FLOW RATE SET | FPA | Substantially Equivalent | Medical Product Specialists | accessdata.fda.gov |
| July 21, 1998 | K982047 | MPS HUBER NEEDLE EXTENSION SET | FPA | Substantially Equivalent | Medical Product Specialists | accessdata.fda.gov |
| July 15, 1998 | K972538 | FLOW-EZE BLUNT CANNULA (1999BC) | FMI | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| February 6, 1996 | K955896 | MACROBORE TUBING - CDC-F-1 THROUGH CDC-F-11 | LHI | Substantially Equivalent | Critical Device Corp. | accessdata.fda.gov |
| February 14, 1992 | K912771 | ACACIAS PHARM/PUMP | LHI | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| July 6, 1990 | K901063 | LUER LOCK TRANSFER PIN | LHI | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| September 12, 1989 | K894217 | SYRINGE TIP ADAPTOR | FMF | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| September 19, 1985 | K853212 | FLOW EASE(PLASTIC VENTED NEEDLE) | LHI | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| April 4, 1985 | K850757 | TANDEM SETS I.V. | LHI | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
| October 31, 1980 | K802561 | HI VOLUME PUMPING CHAMBER | JTB | Substantially Equivalent | Acacia, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Set, I.V. Fluid Transfer
- All makers of Set, Administration, Intravascular
- All makers of System/Device, Pharmacy Compounding
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Piston
Updated November 10, 2010. 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.