Last synced on 20 December 2024 at 11:05 pm

CUFF SENTRY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102674
510(k) Type
Traditional
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2011
Days to Decision
309 days
Submission Type
Statement

CUFF SENTRY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102674
510(k) Type
Traditional
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2011
Days to Decision
309 days
Submission Type
Statement