510(k) K052274 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000
| Applicant | Guidant Corporation, Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 21, 2005 |
| Received | Aug 22, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052274
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 25, 2024 | Maquet Cardiovascular, LLC VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500 Open, Classified |
GEI | None listed |
| Jan 12, 2024 | Maquet Cardiovascular, LLC Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . Open, Classified |
GEI | None listed |
| Dec 6, 2013 | Maquet Cardiovascular, LLC Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470
Indicated for use in minimally invasive surgery allowing access for vessel harves Terminated |
GEI | None listed |
| Sep 20, 2011 | Maquet Cardiovascular, LLC VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System;
Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134.
Product Usage: Endoscopic vessel harvesting systems are indi Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.