Thoracic Catheter Insertion Tray
General, Plastic Surgery · 21 CFR 878.4200
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
- PORTEX THORACIC CATHETERSSep 14, 2020InjurySmiths Medical International, Ltd.3012307300-2020-09257
- PORTEXJun 18, 2020InjurySmiths Medical International, Ltd.3012307300-2020-06067
- PORTEX® THORACIC CATHETERSJul 24, 2019InjurySmiths Medical Asd; Inc.3012307300-2019-02945
- PORTEX® SELDINGER CHEST DRAINAGE KITAug 29, 2018InjurySmiths Medical Asd; Inc.3012307300-2018-03568
- PORTEX THORACIC CATHETERSAug 24, 2018InjurySmiths Medical Asd; Inc.3012307300-2018-03557
Event type breakdown
Most-reported manufacturers
Registered firms
8 firms currently registered for this product code
Synchronis Medical Llc
Romulus, MI, US
Cardinal Health 200, Llc
Waukegan, IL, US
Convertors De Mexico S. De R.l. De C.v
CD.JUAREZ Chihuahua, MX
North American Rescue, Llc.
Greer, SC, US
Integrated Medcraft Llc
East Hampton, CT, US
Cardinal Health 200, Llc
El Paso, TX, US
Sterigenics Us Llc
Grand Prairie, TX, US
Sterigenics U.s., Llc
Charlotte, NC, US
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.