← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

FBNCholedochoscope And Accessories, Flexible/Rigid

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).

DEVICE CLASS
Class II
REGULATION
21 CFR 876.1500
MEDICAL SPECIALTY
Gastroenterology, Urology
REVIEW PANEL
GU
ImplantLife-sustainingGMP-exemptThird-party review eligible
6
510(K)/PMA CLEARANCES
510k: 6
0
RECALL ENTRIES

Recent clearances

K254153Mirco-Tech (Nanjing) Co., Ltd. · 510k2026-04-03
K253139Mirco-Tech (Nanjing) Co., Ltd. · 510k2026-03-19
K251338Scivita Medical Technology Co., Ltd. · 510k2026-01-20
K251170Tangent Endoscopy, LLC · 510k2025-09-12
K243535Shanghai SeeGen Photoelectric Technology Co., Ltd. · 510k2025-03-07
K241444Shenzhen HugeMed Medical Technical Development Co., Ltd. · 510k2025-01-21

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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