510(k) K861862
K861862 is an FDA 510(k) premarket notification submitted by Gil-Med Industries C/O Kegan & Kegan, Ltd. for the device "DIETO CONTAINER FOR ENTERAL NUTRITION". The FDA issued a decision of Substantially Equivalent on Aug 11, 1986. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Gil-Med Industries C/O Kegan & Kegan, Ltd. has 6 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 11, 1986
- Date Received
- May 13, 1986
- 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
- 510(k)