Parke-Davis Co.
Parke-Davis Co. appears in FDA public data with 0 recalls, 47 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 4, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 47
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K861725 | INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT | Dec 4, 1986 |
| K862119 | DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR | Aug 29, 1986 |
| K855120 | ATI DISPOSABLE BIOLOGICAL TEST PACK | Jun 18, 1986 |
| K860570 | ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE | Mar 31, 1986 |
| K860290 | VIAPIC CENTRAL LINE CATHETER | Mar 18, 1986 |
| K852192 | DISPOSABLE STEAM BIOLOGICAL TEST PACK | Nov 1, 1985 |
| K841967 | DESERET THERMODILUTION CARDIAC OUTPUT | Aug 19, 1985 |
| K851327 | DESERET ARTERIAL CATHETER | Jun 14, 1985 |
| K852078 | SPECTRUM(TENTATIVE) | Jun 7, 1985 |
| K844840 | DESERET INTRODUCER SET | May 16, 1985 |
| K850505 | DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER | Mar 11, 1985 |
| K850439 | DESERET EPIDURAL CATHETER | Mar 5, 1985 |
| K843033 | DESERET INTRAVASCULAR CATHETER | Dec 3, 1984 |
| K844219 | DESERET DENTRAL LINE CATHETER | Nov 28, 1984 |
| K844113 | DESERET SUBCLAVIAN JUGULAR CATHETER SET | Nov 28, 1984 |
| K841968 | DESERET DISPOSABLE PRESSURE TRANSDUCER | Aug 6, 1984 |
| K841317 | DESERET HEPARIN COATED FLOW DIRECTED | Jun 11, 1984 |
| K841251 | DESERET HEPARIN COATED FLOW CATH | Jun 11, 1984 |
| K841168 | STERILIZATION PROCESS INDICATOR | May 9, 1984 |
| K840958 | DESERET LONG TERM INDWELLING CATHETER | Apr 17, 1984 |