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FDA 510(k), K122980, GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ
FDA 510(k), K122980, GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ
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510(K) Number: K122980
Device Name: GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ
Manufacturer: Terumo Medical Corporation
Device Classification Name: introducer, catheter
Regulation Number: 870.1340
Classification Product Code: DYB
Date Received: 09/26/2012
Decision Date: 12/11/2012
Regulation Medical Specialty: Cardiovascular
Device Name: GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ
Manufacturer: Terumo Medical Corporation
Device Classification Name: introducer, catheter
Regulation Number: 870.1340
Classification Product Code: DYB
Date Received: 09/26/2012
Decision Date: 12/11/2012
Regulation Medical Specialty: Cardiovascular
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