voss medical products
San Antonio, TX, US
voss medical products appears in FDA device records in San Antonio, TX. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for voss medical products between 1989 and 1993. The busiest year on record is 1989, with 2. The most recent is 1993, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 2 |
| 1990 | 1 |
| 1993 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K932187 | PRONE POSITIONER | KIL | Substantially Equivalent | |
| K932186 | BYPASS LEG POSITIONER | FQO | Substantially Equivalent | |
| K896338 | VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA | DWF | Substantially Equivalent | |
| K885161 | VOSS VEIN CLAMP | DXC | Substantially Equivalent | |
| K895369 | VOSS GRAFT MARKER | KPK | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1643116 | 1643116 | voss medical products | 4235 centergate, San Antonio, TX 78217 US | 2026 | and 7 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- NODBoard, Arm (With Cover), Non-Sterile
- BTXBoard, Arm (With Cover), Sterile
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- DXCClamp, Vascular
- HBMHeadrest, Neurosurgical
- KDDKit, Surgical Instrument, Disposable
- CCWLaryngoscope, Rigid
- KPKMarker, Ostia, Aorto-Saphenous Vein
- NXHNursing Pad, Cohesive Gel
- IQKOrthosis, Cervical
- IQFOrthosis, Cervical-Thoracic, Rigid
- PRNPediatric Position Holder
- KILPositioner, Socket
- FQLStocking, Medical Support (For General Medical Purposes)
- EPWSupport, Head, Surgical, Ent
- CCXSupport, Patient Position
- FQOTable, Operating-Room, Ac-Powered
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
