510(k) K090508
K090508 is an FDA 510(k) premarket notification submitted by Belmont Instrument Corp. for the device "THE BELMONT BUDDY LITE FLUID WARMER". The FDA issued a decision of Substantially Equivalent on March 26, 2009. The device falls under product code BSB (Warmer, Blood, Non-Electromagnetic Radiation), a Class II device regulated under 21 CFR 864.9205. Belmont Instrument Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 26, 2009
- Date Received
- February 26, 2009
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Warmer, Blood, Non-Electromagnetic Radiation
- Device Class
- Class II
- Regulation Number
- 864.9205
- Review Panel
- HE
- Submission Type