510(k) K860703
K860703 is an FDA 510(k) premarket notification submitted by Corning Costar Corp. for the device "U - STAR (MICRO-STAR)". The FDA issued a decision of Substantially Equivalent on May 6, 1986. The device falls under product code LHI (Set, I.V. Fluid Transfer), a Class II device regulated under 21 CFR 880.5440. Corning Costar Corp. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 6, 1986
- Date Received
- February 26, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, I.V. Fluid Transfer
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type