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FDA 510(k), K904573, PENTAX ULTRASOUND ENDOSCOPE, MODEL FG-32UA
FDA 510(k), K904573, PENTAX ULTRASOUND ENDOSCOPE, MODEL FG-32UA
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$149.00 USD
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$149.00 USD
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510(K) Number: K904573
Device Name: PENTAX ULTRASOUND ENDOSCOPE, MODEL FG-32UA
Manufacturer:
Device Classification Name: Endoscopic Ultrasound System, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: ODG
Date Received: 10/09/1990
Decision Date: 06/12/1991
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: PENTAX ULTRASOUND ENDOSCOPE, MODEL FG-32UA
Manufacturer:
Device Classification Name: Endoscopic Ultrasound System, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: ODG
Date Received: 10/09/1990
Decision Date: 06/12/1991
Regulation Medical Specialty: Gastroenterology/Urology
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