Vertex Medical Corp.
Mchenry, IL, US
Vertex Medical Corp. appears in FDA device records in Mchenry, IL. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Vertex Medical Corp. between 1982 and 1984. The busiest year on record is 1982, with 14. The most recent is 1984, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 14 |
| 1983 | 5 |
| 1984 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K833742 | ESCHMANN DILATION CATHETER | Substantially Equivalent | ||
| K834476 | NEPHROSTOMY/BILIARY DRAINAGE BAG | LJE | Substantially Equivalent | |
| K832380 | PROTECTIVE SLEEVE | DYG | Substantially Equivalent | |
| K831666 | SIALOGRAPHY NEEDLE | Substantially Equivalent | ||
| K830576 | LYMPHANGIOGRAPHY SET | DQO | Substantially Equivalent | |
| K830420 | POLYETHYLENE MONITORING CONNECTORS | DQO | Substantially Equivalent | |
| K830237 | TRANSLUCENT POLY. CATH. CONNECTOR AND | DQO | Substantially Equivalent | |
| K823340 | CLEAR VINYL MONITORING CONNECTOR | DXT | Substantially Equivalent | |
| K823256 | ULTRA-ASEPT ANGIOGRAPHIC SYRINGE/SPARE | DXT | Substantially Equivalent | |
| K823254 | REUSABLE METAL STOPCOCK | DXT | Substantially Equivalent | |
| K823253 | VERTEX MONITORING CATHETER | DXT | Substantially Equivalent | |
| K823192 | TUOHY-BORST ADAPTER W/SIDE ARM | DXT | Substantially Equivalent | |
| K823191 | DISPOSABLE PLASTIC STOPCOCK | DXT | Substantially Equivalent | |
| K823190 | BACKSTOP VALVE W/SIDE ARM | DXT | Substantially Equivalent | |
| K823255 | NON-STERILE REUSABLE NEEDLES | FMI | Substantially Equivalent | |
| K822598 | TEFLON PIGTAIL/PERCUTANEOUS CARDIOVAS | DQO | Substantially Equivalent | |
| K822595 | VESSEL DILATOR | DRE | Substantially Equivalent | |
| K822594 | POLYETHYLENE CARDIOVASCULAR CATHETER | DQO | Substantially Equivalent | |
| K822593 | PERCUTANEOUS CATHETER INTRODUCER SET | DYB | Substantially Equivalent | |
| K822597 | GUIDE WIRE | DQX | Substantially Equivalent | |
| K822596 | VERTEX PERCUTANEOUS PUNCTURE NEEDLE | DQO | 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