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Implanted Subcutaneous Securement Catheter

FDA product code OKC · Class 2 · General Hospital

10
Registered devices
18
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lot

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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.