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Pretika

PRETIKA CORPORATION · Model ST261 · UDI-DI 00813859002619

IRONFOGET
10
510(k) clearances
5
Adverse events
2
Recalls
66
Facilities

Description

SonicLift

Recalls

DateFirmReason
2012-05-07Non-Invasive Monitoring Systems, Inc.Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling promotional materials which contain unsubstantiated direct and indirect claims.
2012-05-07Non-Invasive Monitoring Systems, Inc.Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling promotional materials which contain unsubstantiated direct and indirect claims.

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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.