Microvena Corp.
Findley, MN, US
Microvena Corp. appears in FDA device records in Findley, MN. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Microvena Corp. between 1990 and 1999. The busiest year on record is 1990, with 3. The most recent is 1999, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 3 |
| 1991 | 2 |
| 1993 | 2 |
| 1995 | 2 |
| 1996 | 3 |
| 1997 | 1 |
| 1998 | 3 |
| 1999 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K991898 | ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE | DQX | Substantially Equivalent | |
| K991194 | MODIFICATION TO ULTRA-SELECT GUIDEWIRE | DQX | Substantially Equivalent | |
| K982657 | AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100 | MCW | Substantially Equivalent | |
| K970668 | THE AMPLANTZ GOOSE NECK MICROSNARE | DQY | Substantially Equivalent | |
| K972511 | AMPLATZ GOOSE NECK SNARE KIT/ CATHETER | DXE | Substantially Equivalent | |
| K971984 | AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200) | MCW | Substantially Equivalent | |
| K954642 | HYDRO-SELECT GUIDEWIRE | DQX | Substantially Equivalent | |
| K954205 | THE AMPLATZ THROMBECTOMY DEVICE | MCW | Substantially Equivalent | |
| K955304 | CRICKET | DQX | Substantially Equivalent | |
| K952860 | THE NINER NITINOL GUIDEWIRE | DQX | Substantially Equivalent | |
| K946356 | M-PATH NITINOL GUIDEWIRE | DQX | Substantially Equivalent | |
| K925439 | MICROSNARE | DQY | Substantially Equivalent | |
| K922060 | .25' ULTRA-SELECT GUIDEWIRE | DQX | Substantially Equivalent | |
| K914046 | THE BIG EASY Y-ADAPTER | DYB | Substantially Equivalent | |
| K910280 | ULTRA-SELECT PTCA GUIDEWIRE | DQX | Substantially Equivalent | |
| K901502 | AMPLATZ GOOSE-NECK SNARE | DXE | Substantially Equivalent | |
| K900657 | UNIVERSAL DELIVERY SYSTEM CATHETER | DQY | Substantially Equivalent | |
| K896096 | SOLOSTICK (AMPLATZ DILATOR NEEDLE) | DRE | 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