Percutaneous Endoscopic Gastrostomy Kit
The Percutaneous Endoscopic Gastrostomy Kit is a convenience kit containing supplies used for percutaneous endoscopic gastrostomy (PEG) tube placement, a minimally invasive procedure to create a gastrostomy for long-term enteral feeding access. 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 PSG; not an implant and not life-sustaining.
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Basic Information
- Product Code
- PSG
- 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 7 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 7 registration numbers. Click on an entry to view related FDA registrations.