Advocacy International, Ltd.
Mchenry, IL, US
Advocacy International, Ltd. appears in FDA device records in Mchenry, IL. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Advocacy International, Ltd. between 1981 and 1988. The busiest year on record is 1981, with 3. The most recent is 1988, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 3 |
| 1983 | 3 |
| 1984 | 2 |
| 1986 | 3 |
| 1988 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K874027 | LIPASE UV [TOYO] | CHI | Substantially Equivalent | |
| K873792 | SEPACELL R-500 AND SEPACELL R-500A | CAK | Substantially Equivalent | |
| K855251 | MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERS | KDI | Substantially Equivalent | |
| K855212 | ASAHI AM SERIES DIALYZERS | FJI | Substantially Equivalent | |
| K854259 | SEPACELL R-500 & SEPACELL R-500A | CAK | Substantially Equivalent | |
| K842103 | TOYO JOZO URIC ACID TEST | KNK | Substantially Equivalent | |
| K842104 | TOYO JOZO G-GTP TEST | JPZ | Substantially Equivalent | |
| K830231 | ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES | KOC | Substantially Equivalent | |
| K830183 | ASAHI HOLLOW FIBER KIDNEYS NR SERIES | KOC | Substantially Equivalent | |
| K823733 | EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR | KOC | Substantially Equivalent | |
| K813037 | FLOWGUARD CATHETERS & CANNALAE | DWF | Substantially Equivalent | |
| K813035 | POLYSTAN VERTICLUDE BLOOD PUMP | DWB | Substantially Equivalent | |
| K813034 | POLYSTAN HEART LUNG MACHINE SYS | DTQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KOCAccessories, Blood Circuit, Hemodialysis
- KNKAcid, Uric, Uricase (Colorimetric)
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- JPZColorimetric Method, Gamma-Glutamyl Transpeptidase
- DTQConsole, Heart-Lung Machine, Cardiopulmonary Bypass
- FJIDialyzer, Capillary, Hollow Fiber
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- CHILipase-Esterase, Enzymatic, Photometric, Lipase
- CAKMicrofilter, Blood Transfusion
- DWBPump, Blood, Cardiopulmonary Bypass, Roller Type
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain