510(k) K051480
K051480 is an FDA 510(k) premarket notification submitted by Biosearch Medical Products, Inc. for the device "ENTERAL FEEDING TUBE". The FDA issued a decision of Substantially Equivalent on October 12, 2005. The device falls under product code BSS (Tube, Nasogastric), a Class II device regulated under 21 CFR 876.5980. Biosearch Medical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 12, 2005
- Date Received
- June 3, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Nasogastric
- Device Class
- Class II
- Regulation Number
- 876.5980
- Review Panel
- GU
- Submission Type