510(k) K992719
K992719 is an FDA 510(k) premarket notification submitted by Amsino Intl., Inc. for the device "AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE". The FDA issued a decision of Substantially Equivalent on January 12, 2000. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Amsino Intl., Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 12, 2000
- Date Received
- August 12, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubes, Gastrointestinal (And Accessories)
- Device Class
- Class II
- Regulation Number
- 876.5980
- Review Panel
- GU
- Submission Type