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 6 of 6 Results
ProductCode: GYC Applicant: AD-TECH MEDICAL INSTRUMENT CORP. Decision Date To: 05/04/2024
Results per Page
New Search  
Export all 6 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]
dual-sided interhemispheric subdural electrodes, grid subdural electrodes, intraoperative subdural electrodes AD-TECH MEDICAL INSTRUMENT CORP. K053363 05/30/2006
cortical mapping unit, model cmu AD-TECH MEDICAL INSTRUMENT CORP. K992194 09/13/1999
ad-tech subdural electrode AD-TECH MEDICAL INSTRUMENT CORP. K970587 05/09/1997
ad-tech sub dural electrodeds AD-TECH MEDICAL INSTRUMENT CORP. K923803 10/23/1992
ad-tech epidural peg electrode AD-TECH MEDICAL INSTRUMENT CORP. K912760 01/15/1992
wyler subdural strip electrode AD-TECH MEDICAL INSTRUMENT CORP. K850342 07/30/1985
-
-