Irrigation Kit (wounds)
General, Plastic Surgery · 21 CFR 878.4014
This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Recent MDR events
5 adverse event reports on file
- IMPELLA RP PUMP SET, EUMar 10, 2026MalfunctionAbiomed, Inc. - 12206481220648-2026-04920
- IMPELLA RPOct 28, 2024MalfunctionAbiomed, Inc.1220648-2024-21377
- IMPELLA RPSep 15, 2024InjuryAbiomed. Inc.1220648-2024-17936
- IMPELLA RPSep 15, 2024InjuryAbiomed. Inc.1220648-2024-17939
- TRAY,IRR PISTON SYR, 0.9% STRL SALINESep 23, 2019InjuryMedline Industries Inc.1417592-2019-00160
Event type breakdown
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
10 firms currently registered for this product code
Westmed Javid De Mexico, S.a. De C.v.
NOGALES Sonora, MX
Sterigenics Us Llc
Grand Prairie, TX, US
Sterigenics U.s., Llc
Charlotte, NC, US
Cardinal Health 200, Llc
Waukegan, IL, US
Convertors De Mexico S. De R.l. De C.v
CD.JUAREZ Chihuahua, MX
Amsino Medical (kunshan) Co., Ltd.
KUNSHAN CITY Jiangsu, CN
Isomedix Operations Inc
EL PASO, TX, US
Cardinal Health 200, Llc
El Paso, TX, US
Isomedix Operations Inc
El Paso, TX, US
Midwest Sterilization Corp.
JACKSON, MO, US
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.