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DU857 DUAL FREQUENCY ULTRASOUND THERAPY AND MUSCLE STIMULATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052340
510(k) Type
Traditional
Applicant
ALFA TECH MEDICAL SYSTEMS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
105 days
Submission Type
Summary

DU857 DUAL FREQUENCY ULTRASOUND THERAPY AND MUSCLE STIMULATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052340
510(k) Type
Traditional
Applicant
ALFA TECH MEDICAL SYSTEMS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
105 days
Submission Type
Summary