510(k) K953741
K953741 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "THERMACYL BLOOD/FLUID WARMER". The FDA issued a decision of Substantially Equivalent on June 26, 1996. The device falls under product code BSB (Warmer, Blood, Non-Electromagnetic Radiation), a Class II device regulated under 21 CFR 864.9205. Baxter Healthcare Corp has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 26, 1996
- Date Received
- August 10, 1995
- Clearance Type
- Traditional
- 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