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AUGUSTINE GUIDE(TM) KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912690
510(k) Type
Traditional
Applicant
AUGUSTINE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1991
Days to Decision
78 days
Submission Type
Statement

AUGUSTINE GUIDE(TM) KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912690
510(k) Type
Traditional
Applicant
AUGUSTINE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1991
Days to Decision
78 days
Submission Type
Statement