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Catheter, Infusion

FDA product code JCY · Class 1 · General, Plastic Surgery

14
Registered devices
35
Adverse events
3
Recalls
14
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-08-31DePuy Mitek, Inc., a Johnson & Johnson Co.Leakage of FMS gravity tub sets (281113) at the bulb and tube connection
2010-09-10Linvatec Corp. dba ConMed LinvatecOn 09/13/2010 ConMed Linvatec, Largo, FL initiated a recall on 24k100 Arthroscopy Outflow/Suction Tube Set used with the ConMed Linvatec 24k Pump. The 24k100 A
2009-09-01Medical Device Technologies, Inc.Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Ac

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