FDA 510(k), K040981, USW NEEDLEKNIFE PAPILLOTOME

FDA 510(k), K040981, USW NEEDLEKNIFE PAPILLOTOME

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510(K) Number: K040981
Device Name: USW NEEDLEKNIFE PAPILLOTOME
Manufacturer:
Device Classification Name: Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Regulation Number: 876.4300
Classification Product Code: KNS
Date Received: 04/15/2004
Decision Date: 05/07/2004
Regulation Medical Specialty: Gastroenterology/Urology
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