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FDA 510(k), K050159, MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
FDA 510(k), K050159, MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
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$149.00 USD
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510(K) Number: K050159
Device Name: MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
Manufacturer:
Device Classification Name: Stethoscope, Electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 01/25/2005
Decision Date: 02/22/2005
Regulation Medical Specialty: Cardiovascular
Device Name: MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
Manufacturer:
Device Classification Name: Stethoscope, Electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 01/25/2005
Decision Date: 02/22/2005
Regulation Medical Specialty: Cardiovascular
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