Laparoscopic Gastrostomy Kit
The Laparoscopic Gastrostomy Kit is a convenience kit containing supplies used during laparoscopic procedures to create a gastrostomy, a direct opening from the abdominal wall into the stomach, for long-term enteral access in patients requiring tube feeding. It is classified as FDA Class 2 under 21 CFR 876.5980 in the Gastroenterology and Urology specialty. Per the FDA's 1997 Convenience Kits Interim Regulatory Guidance, this kit is under enforcement discretion and does not require a 510(k) premarket notification if it meets all applicable criteria. Product code PSD; not an implant and not life-sustaining.
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Basic Information
- Product Code
- PSD
- Device Class
- FDA class 2
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Review Panel
- GU
- Submission Type
- 7
Device Characteristics
Definition
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.
FEI Numbers
This FDA classification entry is associated with 11 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 11 registration numbers. Click on an entry to view related FDA registrations.