PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000— 510(k) K024036
Substantially EquivalentJohari Digital Healthcare , Ltd.
FDA 510(k) clearance K024036 for PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000, Substantially Equivalent on 2002-12-20. Applicant: Johari Digital Healthcare , Ltd..
Clearance details
- Applicant
- Johari Digital Healthcare , Ltd.
- Product code
- Code IPF
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Jodhpur, Raj, IN
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