Ameco Medical Industries
10TH OF RAMADAN CITY Ash, EG
AMECO MEDICAL INDUSTRIES appears in FDA device records in 10TH OF RAMADAN CITY Ash, EG. FDA records list 6 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 6 510(k) clearances for Ameco Medical Industries between 2011 and 2016. The busiest year on record is 2013, with 3. The most recent is 2016, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2011 | 2 |
| 2013 | 3 |
| 2016 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K152819 | Amecath Peripheral inserted Central Venous Catheter Sets | LJS | Substantially Equivalent | |
| K131144 | AMECO SHEATH INTRODUCER | DYB | Substantially Equivalent | |
| K131814 | AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER | MSD | Unknown | |
| K123943 | AMECATH DUAL LUMEN HEMODIALYSIS CATHETER | MSD | Substantially Equivalent | |
| K110794 | AMECATH CVC AND AMECATH PRESSURE CVC SHORT TERM SINGLE AND MULTI-LUMEN CATHERIZATION KITS | FOZ | Substantially Equivalent | |
| K110793 | AMECATH AND AMECATH UNIQATH SOFT SHORT TERM DUAL HEMODIALYSIS CATHETERIZATION KITS | MPB | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3004134316 | 3004134316 | AMECO MEDICAL INDUSTRIES | INDUSTRIAL AREA B4, 10TH OF RAMADAN CITY Ash Sharqiyah 119 EG | 2026 | and 6 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- GCEAdaptor, Catheter
- MSDCatheter, Hemodialysis, Implanted
- MPBCatheter, Hemodialysis, Non-Implanted
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- GBOCatheter, Nephrostomy, General & Plastic Surgery
- GBWCatheter, Peritoneal
- EYKConnector, Ureteral Catheter
- FENDevice, Cystometric, Hydraulic
- GCCDilator, Catheter
- FFLDislodger, Stone, Basket, Ureteral, Metal
- EYJHolder, Ureteral Catheter
- DYBIntroducer, Catheter
- GCBNeedle, Catheter
- EZBStylet For Catheter, Gastro-Urology
- EYAStylet, Ureteral
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