Last synced on 4 February 2023 at 10:33 pm

RS-4I MUSCLE STIMULATOR FAMILY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062325
510(k) Type
Traditional
Applicant
RS MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2007
Days to Decision
247 days
Submission Type
Summary

RS-4I MUSCLE STIMULATOR FAMILY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062325
510(k) Type
Traditional
Applicant
RS MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2007
Days to Decision
247 days
Submission Type
Summary