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Device For Sealing Microsections

FDA product code KIM · Class 1 · Pathology

72
Registered devices
10
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-09-04Leica Microsystems, Inc.Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shoc

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