Instruments for Cardiac Research
Mchenry, IL, US
Instruments For Cardiac Research appears in FDA device records in Mchenry, IL. FDA records list 8 510(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
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Instruments for Cardiac Research between 1977 and 1984. The busiest year on record is 1982, with 3. The most recent is 1984, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 2 |
| 1981 | 2 |
| 1982 | 3 |
| 1984 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K834397 | HOLTER CARDIOGRAPHY SYS 6201 | DSI | Substantially Equivalent | |
| K821173 | EVENTMASTER 3 HOLTER EVENT SCANNER | DSF | Substantially Equivalent | |
| K820856 | EVENTMASTER 2 | DSI | Substantially Equivalent | |
| K820011 | CARDIOSTRESS | DPS | Substantially Equivalent | |
| K812920 | EVENT MASTER | DSH | Substantially Equivalent | |
| K801903 | SERIES 4000 STRESS & EXERCISE SYSTEM | DSI | Substantially Equivalent | |
| K771374 | SCANNER TREND SYSTEM | DSI | Substantially Equivalent | |
| K770705 | CARDIAC ACQUISITION SYSTEM, ICR 2001 | DQK | 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