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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

DateFirmReason
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.