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Biowave Percutaneous Electrodes

BIOWAVE CORPORATION · Model MK78515 - BWEP02-E · UDI-DI 00859911006027

NHI Prescription
1
510(k) clearances
80
Adverse events
0
Recalls
12
Facilities

Description

Biowave Percutaneous Electrode Set - E

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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.