Last synced on 14 November 2025 at 11:06 pm

AUGUSTINE GUIDE KIT WITH GAUZE SPONGE

Page Type
Cleared 510(K)
510(k) Number
K914168
510(k) Type
Traditional
Applicant
AUGUSTINE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1991
Days to Decision
20 days
Submission Type
Summary

AUGUSTINE GUIDE KIT WITH GAUZE SPONGE

Page Type
Cleared 510(K)
510(k) Number
K914168
510(k) Type
Traditional
Applicant
AUGUSTINE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1991
Days to Decision
20 days
Submission Type
Summary