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ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042619
510(k) Type
Special
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2004
Days to Decision
42 days
Submission Type
Statement

ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042619
510(k) Type
Special
Applicant
SONOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2004
Days to Decision
42 days
Submission Type
Statement