Karl Storz Flexible Choledochoscope

FDA 510(k) K942112 · Karl Storz Endoscopy

Substantially Equivalent

510(k) numberK942112

Submission

Device name
Karl Storz Flexible Choledochoscope
Applicant
Karl Storz Endoscopy
Culver City, CA, US
Received
May 2, 1994
Decision date
February 28, 1995
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 Karl Storz Flexible Choledochoscope cleared by the FDA?

Karl Storz Flexible Choledochoscope (K942112) received a 510(k) decision of Substantially Equivalent on February 28, 1995, 302 days after the submission was received.

What is the product code of K942112?

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