Magnetic Resonance Equipment Corp.
Bay Shore, NY, US
Magnetic Resonance Equipment Corp. appears in FDA device records in Bay Shore, NY. FDA records list 5 510(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
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Magnetic Resonance Equipment Corp. between 1993 and 2001. The busiest year on record is 1993, with 2. The most recent is 2001, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 2 |
| 1997 | 1 |
| 1999 | 1 |
| 2001 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K003982 | TEMPERATURE FUNCTION, MODEL 9500 MULTIGAS MONITOR | CCK | Substantially Equivalent | |
| K983250 | INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR | DSK | Substantially Equivalent | |
| K954120 | MODEL 9500 MR-COMPATIBLE MULTIGAS MONITOR | CCK | Substantially Equivalent | |
| K924285 | MODEL 3500 MR-COMPATIBLE PULSE OXIMETER | DQA | Substantially Equivalent | |
| K924282 | MODEL 320 MR-COMPATIBLE PULSE OXIMETER | DQA | 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