Laparoscopic Gastrostomy Kit
Gastroenterology, Urology · 21 CFR 876.5980
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
0 adverse event reports on file
No MDR events on file for this product code.
Event type breakdown
No data available.
Most-reported manufacturers
No data available.
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
11 firms currently registered for this product code
Honduras Kitting, S.a.
Villanueva Cortes, HN
Isomedix Operations Inc
El Paso, TX, US
Cardinal Health 200, Llc
El Paso, TX, US
Sterigenics U.s., Llc
Charlotte, NC, US
Sterigenics Us Llc
Grand Prairie, TX, US
Convertors De Mexico S. De R.l. De C.v
CD.JUAREZ Chihuahua, MX
Sterigenics U.s., Llc
Ontario, CA, US
Isomedix Operations Inc
EL PASO, TX, US
Cardinal Health 200, Llc
Waukegan, IL, US
Avid Medical, Inc. A Medical Action Ind. Company 305
TOANO, VA, US
Medical Action Industries, Inc. 306
ARDEN, NC, US
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.