Norton Performance Plastics Corp.
Mchenry, IL, US
Norton Performance Plastics Corp. appears in FDA device records in Mchenry, IL. FDA records list 39 510(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
- 39
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 39 510(k) clearances for Norton Performance Plastics Corp. between 1977 and 1985. The busiest year on record is 1982, with 8. The most recent is 1985, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 5 |
| 1978 | 3 |
| 1979 | 4 |
| 1980 | 7 |
| 1981 | 1 |
| 1982 | 8 |
| 1983 | 5 |
| 1984 | 3 |
| 1985 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K853791 | NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000 | DTR | Substantially Equivalent | |
| K852914 | ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION | DQY | Substantially Equivalent | |
| K851299 | CORRECT FLO | FPA | Substantially Equivalent | |
| K842858 | FLUID ADMINISTRATION LINE W/SPIKE 14-923 | FPA | Substantially Equivalent | |
| K841828 | CENTRAL VENOUS CATHETER W/BIG-GARD | DQY | Substantially Equivalent | |
| K840240 | MICROFUSE INTRAVENOUS CATHETER SET | DQY | Substantially Equivalent | |
| K831587 | TEMP. REPAIR KIT-DUAL LUMEN CATHETER | LJS | Substantially Equivalent | |
| K831698 | DISPOSABLE PRESSURE TRANSDUCER#14004195 | DRS | Substantially Equivalent | |
| K830788 | CENTRAL VEIN CATHERIZATION KIT-14-690- | DQO | Substantially Equivalent | |
| K830813 | FRENCH PERCUTANEOUS SHEATH INTRODUCER | DYB | Substantially Equivalent | |
| K830969 | PERM. REPAIR KIT FOR LEONARD NORTON DUAL | LJS | Substantially Equivalent | |
| K821996 | LEONARD PERIPHERAL VENOUS PRESSURE CATH | DYG | Substantially Equivalent | |
| K821679 | LEONARD/NORTON HYPERALIMENTATION CATHET. | FOZ | Substantially Equivalent | |
| K820864 | NORTON MANIFOLD | DTL | Substantially Equivalent | |
| K820710 | NEONATAL INTRODUCER KIT | DYB | Substantially Equivalent | |
| K820677 | TOUCH FLUSH CONTINUOUS FAST/FLUSH | DRS | Substantially Equivalent | |
| K820676 | TOUCH FLUSH W/Y TRANSDUCER CONNECTOR | DRS | Substantially Equivalent | |
| K820581 | NORTON JUGULAR KITS | DYB | Substantially Equivalent | |
| K820229 | NORTON FLOW DIRECTED THERMODILUTION CATH | DYG | Substantially Equivalent | |
| K813137 | CORREC TORR TM | DRS | Substantially Equivalent | |
| K802945 | PRESSURE MONITORING SET | DQO | Substantially Equivalent | |
| K800622 | EXTENSION LINE | DQO | Substantially Equivalent | |
| K800621 | PERCUTANEOUS CATHETER INTRODUCER ADAPTER | DYB | Substantially Equivalent | |
| K800620 | VENOUS M/A INTERNAL JUGULAR KIT | DYB | Substantially Equivalent | |
| K800619 | THERMODILUTION CATHETER INTRO. KIT | DYB | Substantially Equivalent | |
| K800618 | SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET | DQO | Substantially Equivalent | |
| K791512 | CONTINUOUS AMBULATORY DIALYSIS (CAPD) | KDJ | Substantially Equivalent | |
| K791890 | CONTINUOUS FLUSH DEVICE, CAT. #14-370 | KRA | Substantially Equivalent | |
| K791107 | STOPCOCK, THREE WAY | DTL | Substantially Equivalent | |
| K790604 | CUSTOM TUBING SETS | FPA | Substantially Equivalent | |
| K790358 | FLUID ADMINISTRATION CAT.#14-923 | GAZ | Substantially Equivalent | |
| K780985 | PVC LINES FOR MONITORING | GAZ | Substantially Equivalent | |
| K780984 | PVC QUICK PRIME LINES | KRI | Substantially Equivalent | |
| K780662 | SUPPLEMENTAL TYGON PAC-MONITORING LINES | FMG | Substantially Equivalent | |
| K771387 | MONITORING LINES & FLUID ADMIN. | FPK | Substantially Equivalent | |
| K770916 | TYGON PAC-MONITORING LINES & FLUID ADMIN | FMG | Substantially Equivalent | |
| K770708 | TYGON PAC-STOPCOCKS | FMG | Substantially Equivalent | |
| K770707 | TYGON PAC-MONITORING LINES & FLUID ADMIN | FMG | Substantially Equivalent | |
| K770299 | TYGON M-60/TYGON M-70 | FID | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KRIAccessory Equipment, Cardiopulmonary Bypass
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- KRACatheter, Continuous Flush
- DYGCatheter, Flow Directed
- DQOCatheter, Intravascular, Diagnostic
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- DQYCatheter, Percutaneous
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- DYBIntroducer, Catheter
- KDJSet, Administration, For Peritoneal Dialysis, Disposable
- FPASet, Administration, Intravascular
- FMGStopcock, I.V. Set
- DRSTransducer, Blood-Pressure, Extravascular
- FIDTubing, Dialysate
- FPKTubing, Fluid Delivery
- GAZTubing, Noninvasive
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
