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FDA 510(k), K861136, INTERSTIM 100 SYSTEM
FDA 510(k), K861136, INTERSTIM 100 SYSTEM
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510(K) Number: K861136
Device Name: INTERSTIM 100 SYSTEM
Manufacturer: DAVID W SCHLERF
Device Classification Name: Stimulator, Muscle, Powered
Regulation Number: IPF
Classification Product Code: 03/26/1986
Date Received: 07/09/1986
Decision Date: SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty: Physical Medicine
Device Name: INTERSTIM 100 SYSTEM
Manufacturer: DAVID W SCHLERF
Device Classification Name: Stimulator, Muscle, Powered
Regulation Number: IPF
Classification Product Code: 03/26/1986
Date Received: 07/09/1986
Decision Date: SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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