Last synced on 14 November 2025 at 11:06 pm

SCANFLEX SOLID COUPLANT MEMBRANE

Page Type
Cleared 510(K)
510(k) Number
K983691
510(k) Type
Traditional
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1999
Days to Decision
197 days
Submission Type
Statement

SCANFLEX SOLID COUPLANT MEMBRANE

Page Type
Cleared 510(K)
510(k) Number
K983691
510(k) Type
Traditional
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1999
Days to Decision
197 days
Submission Type
Statement