510(k) K953741

THERMACYL BLOOD/FLUID WARMER by Baxter Healthcare Corp — Product Code BSB

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