510(k) K011071
K011071 is an FDA 510(k) premarket notification submitted by Maersk Medical A/S for the device "PARADIGM QUICK-SET INFUSION SET". The FDA issued a decision of Substantially Equivalent on June 7, 2001. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Maersk Medical A/S has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 7, 2001
- Date Received
- April 9, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, Administration, Intravascular
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type