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RENPHO

Joicom Corporation · Model RP-SNM066 · UDI-DI 00810140061515

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

Description

Neck and Shoulder Massager

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.