Catheter Technology Corp.
Walker, MI, US
Catheter Technology Corp. appears in FDA device records in Walker, MI. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Catheter Technology Corp. between 1983 and 1988. The busiest year on record is 1983, with 6. The most recent is 1988, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 6 |
| 1984 | 2 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 2 |
| 1988 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K880571 | CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K871080 | PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER | DQY | Substantially Equivalent | |
| K871998 | GROSHONG CV CATHETER REPAIR KIT | LJS | Substantially Equivalent | |
| K860256 | BRAWN AND GROSHONG CATHETERS | FOZ | Substantially Equivalent | |
| K842577 | CATH-TECH POLYURETHANE UMBILICAL VESS | FOZ | Substantially Equivalent | |
| K842147 | CATH-TECH CHOLANGIOGRAPHY CATHETER | FGE | Substantially Equivalent | |
| K840339 | UMBILICAL VESSEL CATHETER | FOS | Substantially Equivalent | |
| K831386 | GROSHONG CATHETER, LONG TERM TYPE | LJS | Substantially Equivalent | |
| K831366 | TESTCORP PREG | JHJ | Substantially Equivalent | |
| K831365 | TESTCORP ANA | LKS | Substantially Equivalent | |
| K831361 | BETA-PREG | JHJ | Substantially Equivalent | |
| K831362 | TESTCORP CRP | DCN | Substantially Equivalent | |
| K831363 | TESTCORP ASO | GTQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- JHJAgglutination Method, Human Chorionic Gonadotropin
- GTQAntistreptolysin - Titer/Streptolysin O Reagent
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- DQYCatheter, Percutaneous
- FOSCatheter, Umbilical Artery
- LKSDevice, Parasite Concentration
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
- FGEStents, Drains And Dilators For The Biliary Ducts
- DCNSystem, Test, C-Reactive Protein
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