510(k) K790574
K790574 is an FDA 510(k) premarket notification submitted by National Patent Development Corp. for the device "EPIC D215". The FDA issued a decision of Substantially Equivalent on April 30, 1979. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. National Patent Development Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 30, 1979
- Date Received
- March 23, 1979
- 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