Kone Instruments, Inc.
Mchenry, IL, US
Kone Instruments, Inc. appears in FDA device records in Mchenry, IL. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Kone Instruments, Inc. between 1982 and 1987. The busiest year on record is 1982, with 3. The most recent is 1987, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 3 |
| 1983 | 2 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 3 |
| 1987 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K873345 | 'MICROLYTE 4/5' | JFP | Substantially Equivalent | |
| K870777 | PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER | JJF | Substantially Equivalent | |
| K863466 | M700 STRESS MONITOR | DRT | Substantially Equivalent | |
| K862655 | SIGNA II RESTING ECG ELECTRODE | DRX | Substantially Equivalent | |
| K860767 | MODEL E 600 ELECTROCARDIOGRAPH | DSI | Substantially Equivalent | |
| K853354 | MEDIC 4 | LDD | Substantially Equivalent | |
| K840200 | PROGRESS SELECTIVE DHEMISTRY ANALYZ | JJF | Substantially Equivalent | |
| K830433 | PATIENT MONITOR 575 | DRT | Substantially Equivalent | |
| K830432 | CENTRAL STATION 590 | DRT | Substantially Equivalent | |
| K822952 | 560 | DRT | Substantially Equivalent | |
| K820541 | MICROLYTE | JJF | Substantially Equivalent | |
| K820540 | OLLI 565 | DRT | 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