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FDA PRODUCT CODE · CLASS II

QAUHemostatic Device For Endoscopic Gastrointestinal Use

Hemostatic device for intraluminal gastrointestinal use. A hemostatic device for intraluminal gastrointestinal use is a prescription device that is endoscopically applied to the upper and/or lower gastrointestinal tract and is intended to produce hemostasis via absorption of fluid or by other physical means.

DEVICE CLASS
Class II
REGULATION
21 CFR 878.4456
MEDICAL SPECIALTY
General, Plastic Surgery
REVIEW PANEL
SU
ImplantLife-sustainingGMP-exemptThird-party review eligible
4
510(K)/PMA CLEARANCES
510k: 4
0
RECALL ENTRIES

Recent clearances

K253302Wilson-Cook Medical, Inc. · 510k2026-06-02
K2539243-D Matrix Europe SAS · 510k2026-01-07
K240994Nextbiomedical Co., Ltd. · 510k2024-11-27
K2422503-D Matrix Europe SAS · 510k2024-10-22

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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