510(k) K935684
K935684 is an FDA 510(k) premarket notification submitted by Cush Medical Products for the device "IV START KIT". The FDA issued a decision of Substantially Equivalent (kit, denovo) on June 10, 1994. The device falls under product code LRS (I.V. Start Kit), a Class II device regulated under 21 CFR 880.5200. Cush Medical Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SEKD (Substantially Equivalent (kit, denovo))
- Decision Date
- June 10, 1994
- Date Received
- November 29, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- I.V. Start Kit
- Device Class
- Class II
- Regulation Number
- 880.5200
- Review Panel
- SU
- Submission Type
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.