Choledochoscope System

FDA 510(k) K771367 · Richard Wolf Medical Instruments Corp.

Substantially Equivalent

510(k) numberK771367

Submission

Device name
Choledochoscope System
Applicant
Richard Wolf Medical Instruments Corp.
Mchenry, IL, US
Received
July 25, 1977
Decision date
August 2, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Choledochoscope System cleared by the FDA?

Choledochoscope System (K771367) received a 510(k) decision of Substantially Equivalent on August 2, 1977, 8 days after the submission was received.

What is the product code of K771367?

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