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FDA 510(k), K953876, PENTAX ULTRASOUND ENDOSCOPE MODEL FG-32UA (MODIFICATION)
FDA 510(k), K953876, PENTAX ULTRASOUND ENDOSCOPE MODEL FG-32UA (MODIFICATION)
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$149.00 USD
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$149.00 USD
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510(K) Number: K953876
Device Name: PENTAX ULTRASOUND ENDOSCOPE MODEL FG-32UA (MODIFICATION)
Manufacturer:
Device Classification Name: Endoscopic Ultrasound System, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: ODG
Date Received: 08/07/1995
Decision Date: 11/24/1995
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: PENTAX ULTRASOUND ENDOSCOPE MODEL FG-32UA (MODIFICATION)
Manufacturer:
Device Classification Name: Endoscopic Ultrasound System, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: ODG
Date Received: 08/07/1995
Decision Date: 11/24/1995
Regulation Medical Specialty: Gastroenterology/Urology
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