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: KXA
Date Received: 03/26/1986
Decision Date: 07/09/1986
Decision Date: SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty: Physical Medicine
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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