Life Science Instrumentation, Inc.
Mchenry, IL, US
Life Science Instrumentation, Inc. appears in FDA device records in Mchenry, IL. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Life Science Instrumentation, Inc. between 1981 and 1985. The busiest year on record is 1982, with 8. The most recent is 1985, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 6 |
| 1982 | 8 |
| 1983 | 2 |
| 1984 | 2 |
| 1985 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K850812 | EMERGIPACE - EXTERNAL PACEMAKER | DRO | Substantially Equivalent | |
| K842037 | LS 5 | DRT | Substantially Equivalent | |
| K843396 | LS-260G MONITOR/RECORDER & DEFIBILLATOR | LDD | Substantially Equivalent | |
| K840246 | MINI-DEFIBRILLATOR 280/4 | LDD | Substantially Equivalent | |
| K831056 | DEFIBRILLATOR VPD 545 | LDD | Substantially Equivalent | |
| K822617 | VPD540 DEFIBRILLATOR | LDD | Substantially Equivalent | |
| K822616 | LS6 ARRYTHMIA DISCRIMINATOR | DSI | Substantially Equivalent | |
| K822615 | LIFE WATCH LSI | DRT | Substantially Equivalent | |
| K822390 | LIFE TRACE 24 | DRT | Substantially Equivalent | |
| K822389 | LIFE TRACE 40/42 | DRT | Substantially Equivalent | |
| K822294 | VPD-261 DEFIBRILLATOR MONITOR | LDD | Substantially Equivalent | |
| K822388 | LIFE TRACE 14 | DRT | Substantially Equivalent | |
| K821223 | CR-9 | DRT | Substantially Equivalent | |
| K820122 | PIONEER II BACK PLATE ELECTRODE | DRX | Substantially Equivalent | |
| K812520 | 280/4 MINI-DEFIBRILLATOR | LDD | Substantially Equivalent | |
| K812519 | 2000 SERIES PORTABLE RESUSCITATION SYST. | LDD | Substantially Equivalent | |
| K812147 | CARDIORATER CR-7 | DRT | Substantially Equivalent | |
| K812146 | CARDIORATER CR-5 | DRT | Substantially Equivalent | |
| K812145 | CARDIORATER CR-3 | DRT | Substantially Equivalent | |
| K812144 | CENTERAL MONITOR 360 | 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