510(k) K860322
K860322 is an FDA 510(k) premarket notification submitted by Zimmar Consulting , Ltd. for the device "CLINISET INFUSION SET". The FDA issued a decision of Substantially Equivalent on April 7, 1986. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Zimmar Consulting , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 7, 1986
- Date Received
- January 29, 1986
- 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