Eaton Medical Group
Mchenry, IL, US
Eaton Medical Group appears in FDA device records in Mchenry, IL. FDA records list 15 510(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
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Eaton Medical Group between 1983 and 1986. The busiest year on record is 1985, with 12. The most recent is 1986, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1985 | 12 |
| 1986 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K851623 | MODEL TRC-40 TELEMETRY RECIEVER MODULE | DXH | Substantially Equivalent | |
| K851624 | MODEL TT-185 TELEMETRY TRANSMITTER | DXH | Substantially Equivalent | |
| K851625 | SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000 | DSF | Substantially Equivalent | |
| K851632 | PCX-100 PATIENT INPUT LEADWIRE | DRW | Substantially Equivalent | |
| K851627 | KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR | DRW | Substantially Equivalent | |
| K851631 | TMX-C1/C2 TRADMILL CONTROLLER ACCESS. | IOL | Substantially Equivalent | |
| K851630 | TMX-80 TREADMILL | IOL | Substantially Equivalent | |
| K851629 | TMX-70 TREADMILL | IOL | Substantially Equivalent | |
| K851628 | RMG-9 9 REMOTE MONITOR ACCESS. FOR G-2000 ELECTRO | DXJ | Substantially Equivalent | |
| K851633 | CC-100 CLOCK/CALANDER MODULE ACCESS. FOR G-2000 EL | DPS | Substantially Equivalent | |
| K851626 | SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE | DSF | Substantially Equivalent | |
| K850323 | TELEMETRY SOFTWARE FOR G-2000 ELECTROCARDIOGRAPH | DPS | Substantially Equivalent | |
| K850322 | RESTING ECG SOFTWARE FRO G-2000 ELECTROCARDIOGRAPH | DPS | Substantially Equivalent | |
| K850365 | RECORDING ACCESSORY FOR G-2000 EKG MACH. GMP-40 RE | DSF | Substantially Equivalent | |
| K832227 | G-2000 | DPS | 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