Thermal Angel

FDA 510(k) K984640 · Estill Medical Technologies, Inc.

Substantially Equivalent

510(k) numberK984640

Submission

Device name
Thermal Angel
Applicant
Estill Medical Technologies, Inc.
Dallas, TX, US
Received
December 31, 1998
Decision date
July 1, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BSB – Warmer, Blood, Non-Electromagnetic Radiation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.9205
Specialty
Hematology

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K112639The Belmont Buddy Lite Fluid WarmerBSB · Special Belmont Instrument Corp.11/16/2011SE
K090508The Belmont Buddy Lite Fluid WarmerBSB · Special Belmont Instrument Corp.03/26/2009SE
K062774Belmont Buddy Plus Fluid WarmerBSB · Special Belmont Instrument Corp.10/19/2006SE
K052547Belmont Buddy Fluid WarmerBSB · Special Belmont Instrument Corp.10/13/2005SE
K031478MicroheaterBSB · Traditional Belmont Instrument Corp.07/02/2003SE
K020060AstofloBSB · Abbreviated Nats Corp.03/05/2002SE
K012031Modification to Thermal AngelBSB · Special Estill Medical Technologies, Inc.07/26/2001SE
K991159Prismatherm II, AstolineBSB · Abbreviated Stihler Electronic GmbH09/03/1999SE
K991160Astotherm Plus, Astotubes, AstolineBSB · Abbreviated Stihler Electronic GmbH09/02/1999SE
K973741Bair Hugger Blood/Fluid WarmerBSB · Traditional Augustine Medical, Inc.04/30/1998SE

More from Augustine Medical, Inc.

510(k)DeviceDecision
K012031Modification to Thermal AngelBSB · Special 07/26/2001SE

Questions and answers

When was Thermal Angel cleared by the FDA?

Thermal Angel (K984640) received a 510(k) decision of Substantially Equivalent on July 1, 1999, 182 days after the submission was received.

What is the product code of K984640?

The FDA product code is BSB – Warmer, Blood, Non-Electromagnetic Radiation, a Class II (moderate risk) device regulated under 21 CFR 864.9205.