Vasamedics, LLC
Minneapolis, MN, US
Vasamedics, LLC appears in FDA device records in Minneapolis, MN. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Vasamedics, LLC between 1991 and 1997. The busiest year on record is 1991, with 2. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 2 |
| 1995 | 1 |
| 1996 | 2 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K962700 | VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT | DPT | Substantially Equivalent | |
| K961368 | TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT | DPT | Unknown | |
| K951832 | LASERFLO BLOOD PERFUSION SINGLE USE PROBES MODELS SUP-440, SUPR-434 SUP-433 | DPT | Substantially Equivalent | |
| K951486 | MODEL PV2000 VASCULAR MICROLABORATORY | DPW | Substantially Equivalent | |
| K912446 | MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM2 | DPW | Substantially Equivalent | |
| K911763 | LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2) | DPW | 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