FDA Device Intelligence
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Graft, Bypass, Coronary Artery

FDA product code NAV · Class f · Unknown

0
Registered devices
1
Adverse events
3
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2011-06-24The Anspach Effort, Inc.The RPM of the Motor Handpiece may be less than 80,000 RPM.
2011-06-24The Anspach Effort, Inc.The RPM of the Motor Handpiece may be less than 80,000 RPM.
2011-06-24The Anspach Effort, Inc.The RPM of the Motor Handpiece may be less than 80,000 RPM.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.