Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Warmer, Thermal, Infusion Fluid
510(k) Number K896018
Device Name BIOTEMP
Applicant
Medadvances, Inc.
3414 22nd. St.
Lubbock,  TX  79410
Applicant Contact PATRICK GRIFFIN
Correspondent
Medadvances, Inc.
3414 22nd. St.
Lubbock,  TX  79410
Correspondent Contact PATRICK GRIFFIN
Regulation Number880.5725
Classification Product Code
LGZ  
Date Received10/16/1989
Decision Date 02/09/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-