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Cook
Model G14232 · COOK INCORPORATED · DI 00827002142329
FDX — Endoscopic Cytology Brush · Class II · 21 CFR 876.1500
UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
0
27
2019-02
0
12
2019-03
0
24
2019-04
0
6
2019-05
0
12
2019-06
0
9
2019-07
0
6.5
2019-10
0
9
2019-11
0
15.33
2019-12
0
3.67
2020-02
0
2
2020-03
0
1
2020-04
0
3
2020-06
0
1
2020-07
0
3
2020-09
0
2
2020-10
0
1
2020-11
0
1
2020-12
0
2
2021-02
0
1
2021-03
0
6
2021-04
0
3
2021-06
0
3
2021-08
0
3
2021-09
0
2
2021-10
0
2
2021-11
0
3
2022-01
0
9
2022-03
0
2
2022-04
0
3
2022-05
0
3
2022-06
0
3
2022-08
0
1
2022-09
0
3
2022-10
0
6
2023-02
0
1
2023-03
0
3.5
2023-04
0
2
2023-08
0
3
2023-10
0
2
2023-12
0
3
2024-02
0
3
2024-03
0
6
2024-05
0
3
2024-07
0
1.5
2024-09
0
1.67
2024-10
0
2
2024-12
0
2
2025-01
0
3
2025-02
0
3
2025-03
0
3
2025-10
0
3
2025-12
0
2
2026-04
0
2.5
2026-05
0
6
This device (reports/month)Average device in FDX (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — COOK INCORPORATED