Acacia, Inc.
Brea, CA, US
Acacia, Inc. appears in FDA device records in Brea, CA. FDA records list 17 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Acacia, Inc. between 1979 and 2014. The busiest year on record is 1985, with 3. The most recent is 2014, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 1 |
| 1985 | 3 |
| 1989 | 2 |
| 1990 | 2 |
| 1992 | 1 |
| 1993 | 1 |
| 1998 | 1 |
| 2009 | 1 |
| 2010 | 1 |
| 2012 | 1 |
| 2013 | 1 |
| 2014 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K142527 | Extension Set with BD Q-Syte Luer Access Split Septum | FPA | Substantially Equivalent | |
| K122449 | ENTERAL NUTRITION WARMER | LGZ | Substantially Equivalent | |
| K111381 | MEDI-SIS SYRINGE INFUSION SYSTEM | LZH | Substantially Equivalent | |
| K103165 | BLOOD SAMPLING SET | FPA | Substantially Equivalent | |
| K092986 | ACACIA PISTON SYRINGE | FMF | Substantially Equivalent | |
| K972538 | FLOW-EZE BLUNT CANNULA (1999BC) | FMI | Substantially Equivalent | |
| K931095 | SPRING LOADED SYRINGE | FMF | Substantially Equivalent | |
| K912771 | ACACIAS PHARM/PUMP | LHI | Substantially Equivalent | |
| K901063 | LUER LOCK TRANSFER PIN | LHI | Substantially Equivalent | |
| K896990 | PHARMULATOR | LHI | Substantially Equivalent | |
| K894206 | INTOPO | FMF | Substantially Equivalent | |
| K894217 | SYRINGE TIP ADAPTOR | FMF | Substantially Equivalent | |
| K853212 | FLOW EASE(PLASTIC VENTED NEEDLE) | LHI | Substantially Equivalent | |
| K850757 | TANDEM SETS I.V. | LHI | Substantially Equivalent | |
| K850962 | OPHTHALMIC DROPPER BOTTLES | Substantially Equivalent | ||
| K802561 | HI VOLUME PUMPING CHAMBER | JTB | Substantially Equivalent | |
| K782113 | CAP, TAMPER PROOF PLASTIC | KPE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain