Applied Medical Research
Mchenry, IL, US
Applied Medical Research appears in FDA device records in Mchenry, IL. FDA records list 22 510(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
- 22
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 22 510(k) clearances for Applied Medical Research between 1977 and 1980. The busiest year on record is 1978, with 9. The most recent is 1980, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 7 |
| 1978 | 9 |
| 1979 | 5 |
| 1980 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K800025 | DINAMAP RESEARCH MONITOR 1245 | DXN | Substantially Equivalent | |
| K791580 | CEREBRAL FUNCTION MONITOR 870 | OMA | Substantially Equivalent | |
| K791159 | DINAMAP MODEL 855 | DXN | Substantially Equivalent | |
| K790322 | OPTIONAL ACCESSORY FOOT SWITCH MODEL 100 | EBW | Substantially Equivalent | |
| K790328 | MODEL 1051, MONITOR | DXN | Substantially Equivalent | |
| K782073 | DINAMAP MODELS 1160 AND 1165 | DSK | Substantially Equivalent | |
| K781064 | DINAMAP MODEL 848 | DSK | Substantially Equivalent | |
| K781053 | DINAMAP MODEL 846 | DSK | Substantially Equivalent | |
| K781311 | ELECTRODE, NEEDLE, CFM | GXZ | Substantially Equivalent | |
| K780754 | NEONATAL MONITOR | DXN | Substantially Equivalent | |
| K780759 | MODEL 902 STAND | FSH | Substantially Equivalent | |
| K780358 | ACCES. ANALOG OUTPUT ADAPTOR MODEL 910 | DXN | Substantially Equivalent | |
| K780128 | BLOOD PRESSURE MONITOR, ARTERIAL | DRS | Substantially Equivalent | |
| K780127 | DINAMAP MODEL 850 | DRS | Substantially Equivalent | |
| K771981 | MINIMAP MODEL 810 | DSK | Substantially Equivalent | |
| K771932 | RECORDER, DINMAP, MODEL 950 | DSH | Substantially Equivalent | |
| K771931 | MONITOR, DINMAP, MODEL 850 | DXN | Substantially Equivalent | |
| K771897 | DINAMAP MODEL 837 | DXN | Substantially Equivalent | |
| K771896 | DINAMAP MODEL 835 | DXN | Substantially Equivalent | |
| K771895 | DINAMAP MADEL 845 | DXN | Substantially Equivalent | |
| K771782 | DINIMAP MODEL 827A | DXN | Substantially Equivalent | |
| K771772 | DINAMAP MODEL 825A | DSK | 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain