American Viggo
Mchenry, IL, US
American Viggo appears in FDA device records in Mchenry, IL. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for American Viggo between 1976 and 1977. The busiest year on record is 1977, with 6. The most recent is 1977, with 6.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 4 |
| 1977 | 6 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K771339 | MALE LUER LOCK PLUG | FPA | Substantially Equivalent | |
| K770528 | NEEDLE, MEMBRANE | FMI | Substantially Equivalent | |
| K770181 | I.V. CATHETER PLACEMENT UNIT | FOZ | Substantially Equivalent | |
| K770174 | LUER-LOCK EXTENSION SET | FPK | Substantially Equivalent | |
| K770154 | 3-WAY STOPCOCK WITH LUER-LOCK FITTING | KGZ | Substantially Equivalent | |
| K770096 | EPIDURAL BLOCK PROCEDURE PACK | CAZ | Substantially Equivalent | |
| K760679 | 4-WAY STOPCOCK W/7CM TUBING, | FMG | Substantially Equivalent | |
| K760678 | 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK | FMG | Substantially Equivalent | |
| K760667 | 4-WAY STOPCOCK W/10 CM EXTEN. TUBING | FMG | Substantially Equivalent | |
| K760666 | 4-WAY STOPCOCK W/LUER-LOCK FITTING | FMG | 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