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Percutaneous Endoscopic Gastrostomy Kit

FDA product code PSG · Class 2 · Gastroenterology, Urology

6
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-03-16Avanos Medical, Inc.The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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