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Veinsite
Spirometrics · Model VTS1000 · UDI-DI 00855784004009
KZA
Prescription
6
510(k) clearances
19
Adverse events
2
Recalls
27
Facilities
Description
Near infrared vein locator device with a liquid crystal display.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-03-14 | Christie Medical Holding Inc | Instrument may tip over if not moved correctly. |
| 2012-03-14 | Christie Medical Holding Inc | Instrument may tip over if not moved correctly. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
