510(k) K911868
K911868 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "INTERLINK(TM) BLUNT CANNULA, MODIFICATION". The FDA issued a decision of Substantially Equivalent on Jun 24, 1991. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 24, 1991
- Date Received
- Apr 26, 1991
- 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
- 510(k)