Xanmed Corp.
Washington, DC, US
Xanmed Corp. appears in FDA device records in Washington, DC. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Xanmed Corp. between 1984 and 1987. The busiest year on record is 1985, with 6. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 2 |
| 1985 | 6 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K864623 | OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT | KNA | Substantially Equivalent | |
| K844595 | ORTHOPEDIC CUSTOM SURGICAL KIT | LXH | Substantially Equivalent | |
| K844596 | EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT | Unknown | ||
| K844593 | CARDIOVASCULAR CUSTOM SURGICAL KIT | DYB | Substantially Equivalent | |
| K844594 | NEURO CUSTOM SURGICAL KIT | HBA | Substantially Equivalent | |
| K851906 | SURGICAL EYE PACK | HMP | Substantially Equivalent | |
| K844597 | MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT | Substantially Equivalent | ||
| K843642 | SUBCLAVIAN LEAD INTRODUCER SYS | DYB | Substantially Equivalent | |
| K843641 | CATHETER INTRODUCER SYSTEM | DYB | 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
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