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Impulse 7000DP
FLUKE ELECTRONICS CORPORATION · Model IMPULSE 7000DP · UDI-DI 00850540007126
10
510(k) clearances
5
Adverse events
1
Recalls
4
Facilities
Description
Defibrilator/AED Tester, External Pacer Analyzer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-10-28 | BC Group International Inc | Device is not functioning as intended: Two wires running to the ECG distribution circuit board are reversed resulting in inverted waveforms. |
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Get your free API keyRead the docsData 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.