Last synced on 23 September 2022 at 11:05 pm

STASIS BUTTON PRSSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912765
510(k) Type
Traditional
Applicant
ARCH DEVELOPMENT GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1991
Days to Decision
49 days
Submission Type
Statement

STASIS BUTTON PRSSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912765
510(k) Type
Traditional
Applicant
ARCH DEVELOPMENT GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1991
Days to Decision
49 days
Submission Type
Statement