American Mcgaw
Mchenry, IL, US
American Mcgaw 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 American Mcgaw between 1981 and 1985. The busiest year on record is 1981, with 4. The most recent is 1985, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 4 |
| 1982 | 2 |
| 1983 | 1 |
| 1984 | 4 |
| 1985 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K853549 | MCGAW/DROP WATCH FLOW MONITOR | FLN | Substantially Equivalent | |
| K843639 | ADD-A-VIAL SOLUTION TRANSFER DEVICE | LHI | Substantially Equivalent | |
| K843954 | MIXING CONTAINER | KPE | Substantially Equivalent | |
| K841729 | ACCUPRO ENTERAL FEEDING PUMP | FRN | Substantially Equivalent | |
| K840388 | PAB IV CONTAINER | KPE | Substantially Equivalent | |
| K840212 | CONCENTRATED PLATELET ADMIN. SET | FPA | Substantially Equivalent | |
| K831716 | CAPD - CATHETER ADAPTER | FKX | Substantially Equivalent | |
| K822240 | ETHYLENE OXIDE STERILIZ. PARAMETRIC REL. | KFX | Substantially Equivalent | |
| K820133 | MCGAW FAT EMULSION SET | FPA | Substantially Equivalent | |
| K813092 | ACCUPRO I.V. ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K810683 | CAPD CATHETER ADAPTER | FKX | Substantially Equivalent | |
| K810757 | I.V. ADMINISTRATION SET | FDA | Substantially Equivalent | |
| K810600 | CAPD EXCHANGE SET | KDJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KFXAssembly, Thigh/Knee/Shank/Ankle/Foot, External
- KPEContainer, I.V.
- FDAEnteroscope And Accessories
- FLNMonitor, Electric For Gravity Flow Infusion Systems
- FRNPump, Infusion
- KDJSet, Administration, For Peritoneal Dialysis, Disposable
- FPASet, Administration, Intravascular
- LHISet, I.V. Fluid Transfer
- FKXSystem, Peritoneal, Automatic Delivery
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