Last synced on 30 September 2022 at 11:05 pm

5.0 MHZ CONVEX ARRAY INTRAVAGINAL TRANSDUCER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895647
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1989
Days to Decision
89 days

5.0 MHZ CONVEX ARRAY INTRAVAGINAL TRANSDUCER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895647
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1989
Days to Decision
89 days