Venospital, Inc.
Mchenry, IL, US
Venospital, Inc. appears in FDA device records in Mchenry, IL. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Venospital, Inc. between 1977 and 1979. The busiest year on record is 1978, with 7. The most recent is 1979, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 3 |
| 1978 | 7 |
| 1979 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K791131 | FLU VEN TR-1 | KSB | Substantially Equivalent | |
| K791130 | FLU-VEN TK-2 | KSB | Substantially Equivalent | |
| K790424 | FLU-VEN 01510 | FPA | Substantially Equivalent | |
| K790077 | BIOSTIL # 3884 | FPA | Substantially Equivalent | |
| K781190 | INFUSION SET, VENOTHIN 21 | FPA | Substantially Equivalent | |
| K781189 | FLU VEN 0151 | FPA | Substantially Equivalent | |
| K781188 | INFUSION SET, VENOTHIN 25 | FPA | Substantially Equivalent | |
| K781187 | INFUSION SET W/ INJECTION SITE, 23D-W | FPA | Substantially Equivalent | |
| K781186 | INFUSION, VENOTHIN 23 | FPA | Substantially Equivalent | |
| K781185 | INFUSION SET W/ INJECTION SITE | FPA | Substantially Equivalent | |
| K781184 | INFUSION SET, VENOTHIN 19 | FPA | Substantially Equivalent | |
| K771362 | FLU VEN 0150 | FPA | Substantially Equivalent | |
| K770864 | HEMODIALYSIS FISTULA SET | FIE | Substantially Equivalent | |
| K770863 | FLU VEN 0160 | FPA | 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