Cardiac Resucitator Corp.
Mchenry, IL, US
Cardiac Resucitator Corp. appears in FDA device records in Mchenry, IL. FDA records list 17 510(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
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Cardiac Resucitator Corp. between 1981 and 1988. The busiest year on record is 1982, with 5. The most recent is 1988, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 1 |
| 1982 | 5 |
| 1984 | 3 |
| 1985 | 3 |
| 1987 | 4 |
| 1988 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K882513 | MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR | DSI | Substantially Equivalent | |
| K871971 | MODIFIED PACE*AID MODEL 53 | DRO | Substantially Equivalent | |
| K871538 | STAT-PAD (TM) | DRO | Substantially Equivalent | |
| K871569 | MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR | DRO | Substantially Equivalent | |
| K870622 | HEART*AID 1000 | MKJ | Substantially Equivalent | |
| K850596 | PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY & | DRO | Substantially Equivalent | |
| K850170 | HEART AID MODEL 97 | DRO | Substantially Equivalent | |
| K844811 | PACE AID MODEL 53 | DRO | Substantially Equivalent | |
| K843547 | PACE *AID MODEL 52 | DRO | Substantially Equivalent | |
| K843358 | HEART-AID MODEL 80 | DRO | Substantially Equivalent | |
| K841556 | HEART - AID ALS, 95 | LDO | Substantially Equivalent | |
| K821673 | HEART*AID, ALS, MODEL 95 | DRO | Substantially Equivalent | |
| K821152 | HEART AID #90 | DRO | Substantially Equivalent | |
| K820609 | HEART *AID, #80 | DRO | Substantially Equivalent | |
| K820507 | PACE* AID MODEL 50 | DRO | Substantially Equivalent | |
| K813553 | PACE *AID | DRO | Substantially Equivalent | |
| K811028 | PACE AID | Unknown |
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
