Midwest Rf, LLC
Hartland, WI, US
Midwest Rf, LLC appears in FDA device records in Hartland, WI. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Midwest Rf, LLC between 2000 and 2011. The busiest year on record is 2000, with 4. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 4 |
| 2003 | 1 |
| 2005 | 1 |
| 2009 | 1 |
| 2010 | 1 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K111259 | SV DBS VRAIN ARRAY | MOS | Substantially Equivalent | |
| K091496 | MEP-90 HAIR GROWTH STIMULATION SYSTEM | OAP | Substantially Equivalent | |
| K090267 | SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 | MOS | Substantially Equivalent | |
| K051618 | SPECIAL PROCEDURES II HEAD COIL, MODEL 1400GE-64 | MOS | Substantially Equivalent | |
| K030317 | MODEL 1300GE-64: PEDIATRIC POSITIONER | MOS | Substantially Equivalent | |
| K003386 | SPECIAL PROCEDURES HEAD COIL; MODEL # 1100GE-64 | MOS | Substantially Equivalent | |
| K003097 | BRAIN COIL, MODEL 9800GE-64 | MOS | Substantially Equivalent | |
| K002860 | MODEL 6900GE-64: C-SPINE ARRAY | MOS | Substantially Equivalent | |
| K002864 | MODEL 6600GE-64: TRAMA NECK ARRAY | MOS | 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