Last synced on 25 January 2026 at 3:41 am

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024036
510(k) Type
Special
Applicant
Johari Digital Healthcare , Ltd.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
14 days
Submission Type
Summary

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024036
510(k) Type
Special
Applicant
Johari Digital Healthcare , Ltd.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
14 days
Submission Type
Summary