510(k) K880767
K880767 is an FDA 510(k) premarket notification submitted by Medical Innovations Corp. for the device "MIC NEEDLE JEJUNOSTOMY TUBE KIT". The FDA issued a decision of Substantially Equivalent on August 11, 1988. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Medical Innovations Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 11, 1988
- Date Received
- February 26, 1988
- 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