• 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 3 of 3 Results
ProductCode: GXQ Applicant: BIO-VASCULAR, INC. Decision Date To: 05/14/2024
Results per Page
New Search  
Export all 3 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]
dura-guard - dural repair patch BIO-VASCULAR, INC. K982282 07/30/1998
dura-guard-dural repair patch BIO-VASCULAR, INC. K973706 12/24/1997
dura-guard dural repair patch, dura-guard dura substitute BIO-VASCULAR, INC. K950956 06/02/1995
-
-