Chemotherapy Administration Kit
The Chemotherapy Administration Kit is a general hospital convenience kit containing the tubing, connectors, and accessories needed to safely administer chemotherapy agents to patients through intravenous or other routes, providing the necessary components for drug delivery in oncology care. Product code PWS is established as a convenience kit under FDA's 1997 Convenience Kits Interim Regulatory Guidance and is under enforcement discretion, not requiring a 510(k) if all guidance criteria are met. It is classified as FDA Class I under regulation 21 CFR 880.6250, subject only to general controls. It falls under the General Hospital medical specialty and is not flagged as an implant or life-sustaining device.
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Basic Information
- Product Code
- PWS
- Device Class
- FDA class 1
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Review Panel
- HO
- 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 1 FEI number. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 1 registration number. Click on an entry to view related FDA registrations.