510(k) K873464
K873464 is an FDA 510(k) premarket notification submitted by Van Dellen, Ltd. for the device "VAN DELLEN CANNULA". The FDA issued a decision of Substantially Equivalent on November 23, 1987. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Van Dellen, Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 23, 1987
- Date Received
- August 28, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter And Tip, Suction
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type