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Impulse 7010

FLUKE ELECTRONICS CORPORATION · Model IMPULSE 7010 · UDI-DI 00850540007140

DRL
1
510(k) clearances
5
Adverse events
1
Recalls
4
Facilities

Description

Defibrillator Selectable Load Accessory

Recalls

DateFirmReason
2015-10-28BC Group International IncDevice is not functioning as intended: Two wires running to the ECG distribution circuit board are reversed resulting in inverted waveforms.

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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.