510(k) K954983
K954983 is an FDA 510(k) premarket notification submitted by Distronic Sterile Products, Inc. for the device "EXTENSION SET WITH CHECK VALVE". The FDA issued a decision of Substantially Equivalent on January 23, 1996. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Distronic Sterile Products, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 23, 1996
- Date Received
- October 31, 1995
- 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