URF-P2 Ureterorenofiberscope/Choledochofiberscope

FDA 510(k) K912120 · Olympus Corp.

Substantially Equivalent

510(k) numberK912120

Submission

Device name
URF-P2 Ureterorenofiberscope/Choledochofiberscope
Applicant
Olympus Corp.
Lake Success, NY, US
Received
May 14, 1991
Decision date
August 7, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 URF-P2 Ureterorenofiberscope/Choledochofiberscope cleared by the FDA?

URF-P2 Ureterorenofiberscope/Choledochofiberscope (K912120) received a 510(k) decision of Substantially Equivalent on August 7, 1991, 85 days after the submission was received.

What is the product code of K912120?

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