Rectal Dilator Kit
The Rectal Dilator Kit is a convenience kit containing supplies used to dilate the rectum for therapeutic or diagnostic purposes, such as treating rectal strictures or preparing for anorectal procedures, in the Gastroenterology and Urology specialty. It is classified as FDA Class 1 under 21 CFR 876.5450, subject only to general controls. 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 PSJ; not an implant and not life-sustaining.
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Basic Information
- Product Code
- PSJ
- Device Class
- FDA class 1
- Regulation Number
- 876.5450
- 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.