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Pulse Scientific Inc.

Pulse Scientific Inc · Model 10603 · UDI-DI 00628055726005

GMQ
10
510(k) clearances
35
Adverse events
0
Recalls
17
Facilities

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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.