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
-
1 to 7 of 7 Results
ProductCode: GXI Applicant: BAYLIS MEDICAL CO., INC. Decision Date To: 04/25/2024
Results per Page
New Search  
Export all 7 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
duocool pain management probe, model osp-17-180-20 BAYLIS MEDICAL CO., INC. K101372 08/10/2010
pain management optima, model pmo21-100-05, pmo20-100-10cs, pmo20-145-10cs BAYLIS MEDICAL CO., INC. K092337 10/16/2009
baylis pain management single-use probe BAYLIS MEDICAL CO., INC. K071745 07/19/2007
transdiscal system, models tdp-17-150-6, tdi-17-150, tda-ppu-1, tda-tbk-1, tdx-y-tsw-tdp, tdx-pmg-ppu BAYLIS MEDICAL CO., INC. K062937 01/08/2007
baylis pain management cooled probe, model pmpc-18-150-6 BAYLIS MEDICAL CO., INC. K053082 11/30/2005
baylis pain management probe/pmp-20-145 and baylis pain management connector cable/pmx-bay-bay BAYLIS MEDICAL CO., INC. K002389 10/23/2000
bmc rf cannula BAYLIS MEDICAL CO., INC. K972846 07/17/1998
-
-