FDA 510(k), K041934, 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
FDA 510(k), K041934, 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
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510(K) Number: K041934
Device Name: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
Manufacturer:
Device Classification Name: Stethoscope, Electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 07/19/2004
Decision Date: 10/15/2004
Regulation Medical Specialty: Cardiovascular
Device Name: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
Manufacturer:
Device Classification Name: Stethoscope, Electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 07/19/2004
Decision Date: 10/15/2004
Regulation Medical Specialty: Cardiovascular