Last synced on 25 April 2025 at 11:05 pm

SONOSCAPE SSI-1000/SSI-5000 ULTRASOUND TRANSDUCERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052042
510(k) Type
Traditional
Applicant
SONOSCAPE COMPANY LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2005
Days to Decision
12 days
Submission Type
Summary

SONOSCAPE SSI-1000/SSI-5000 ULTRASOUND TRANSDUCERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052042
510(k) Type
Traditional
Applicant
SONOSCAPE COMPANY LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2005
Days to Decision
12 days
Submission Type
Summary