Alien RX Micro Cannula, Model 4530

FDA 510(k) K010993 · Boston Scientific Corp

Substantially Equivalent

510(k) numberK010993

Submission

Device name
Alien RX Micro Cannula, Model 4530
Applicant
Boston Scientific Corp
Natick,, MA, US
Received
April 3, 2001
Decision date
April 30, 2001
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ODD – Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To identify stones, tumors, or narrowing in the biliary tree.

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K963051Ercp CannulaODD · Traditional United States Endoscopy Group, Inc.03/28/1997SE
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K950729Olympus PR-23Q Disposable Cannula (Ball Tip)ODD · Traditional Olympus America, Inc.03/17/1995SE

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Questions and answers

When was Alien RX Micro Cannula, Model 4530 cleared by the FDA?

Alien RX Micro Cannula, Model 4530 (K010993) received a 510(k) decision of Substantially Equivalent on April 30, 2001, 27 days after the submission was received.

What is the product code of K010993?

The FDA product code is ODD – Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula, a Class II (moderate risk) device regulated under 21 CFR 876.1500.