SpyGlass Discover Digital Catheter, SpyGlass Discover Digital Controller

FDA 510(k) K200483 · Boston Scientific Corporation

Substantially Equivalent

510(k) numberK200483

Submission

Device name
SpyGlass Discover Digital Catheter, SpyGlass Discover Digital Controller
Applicant
Boston Scientific Corporation
Marlboro, MA, US
Received
February 27, 2020
Decision date
May 21, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBN – Choledochoscope And Accessories, Flexible/Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

to examine and perform procedures within the bile ducts. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was SpyGlass Discover Digital Catheter, SpyGlass Discover Digital Controller cleared by the FDA?

SpyGlass Discover Digital Catheter, SpyGlass Discover Digital Controller (K200483) received a 510(k) decision of Substantially Equivalent on May 21, 2020, 84 days after the submission was received.

What is the product code of K200483?

The FDA product code is FBN – Choledochoscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.