510(k) K030315 ยท KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM
| Applicant | Ultroid, LLC, Carson City NV, US |
| Decision | Substantially Equivalent, Feb 27, 2003 |
| Received | Jan 30, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030315
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 19, 2016 | Ultroid Technologies, Inc. Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes Terminated |
KNS | None listed |
| Oct 19, 2016 | Ultroid Technologies, Inc. Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes Terminated |
KNS | None listed |
| Oct 19, 2016 | Ultroid Technologies, Inc. Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes. Terminated |
KNS | None listed |
| Oct 19, 2016 | Ultroid Technologies, Inc. Ultroid Sterile Disposable Probes sold individually Terminated |
KNS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.