Olympus CHF Type Y0003

FDA 510(k) K093507 · Olympus Medical Systems Corporation

Substantially Equivalent

510(k) numberK093507

Submission

Device name
Olympus CHF Type Y0003
Applicant
Olympus Medical Systems Corporation
Center Valley, PA, US
Received
November 13, 2009
Decision date
March 10, 2010
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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K231105Flexible Choledochoscope (Model: CS50H-20EU, CS50H-20US)FBN · Traditional Shanghai AnQing Medical Instrument Co., Ltd.10/17/2023SE
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More from Zhuhai Pusen Medical Technology Co., Ltd.

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K2620794K Camera Head OLYMPUS CH-S700-08-LBFET · Traditional 09/10/2026SE
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K260401Evis Eus Ultrasound Bronchofibervideoscope Olympus BF-UCP190F (BF-UCP190F)PSV · Traditional 08/27/2026SE
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K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35…GEI · Traditional 07/01/2026SE
K261260HD Camera Head OLYMPUS CH-S200-08-LBFET · Traditional 06/24/2026SE
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Questions and answers

When was Olympus CHF Type Y0003 cleared by the FDA?

Olympus CHF Type Y0003 (K093507) received a 510(k) decision of Substantially Equivalent on March 10, 2010, 117 days after the submission was received.

What is the product code of K093507?

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