Last synced on 25 April 2025 at 11:05 pm

SONOSCAPE ULTRASOUND SYSTEM AND TRANSDUCERS MODEL SSI-8000, 2P1 PHASED ARRAY, 5P1 PHASED ARRAY MODEL 2P1, 5P1, 6V1 MICRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102642
510(k) Type
Traditional
Applicant
SONOSCAPE COMPANY LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2011
Days to Decision
172 days
Submission Type
Summary

SONOSCAPE ULTRASOUND SYSTEM AND TRANSDUCERS MODEL SSI-8000, 2P1 PHASED ARRAY, 5P1 PHASED ARRAY MODEL 2P1, 5P1, 6V1 MICRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102642
510(k) Type
Traditional
Applicant
SONOSCAPE COMPANY LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2011
Days to Decision
172 days
Submission Type
Summary