510(k) Report

510(k) · Decided

Recalled · Class II · 2016

Customed Cysto Pack I

K902274510(k) TraditionalDecided Sep 20, 1990122-day reviewClass II21 CFR 876.1500Recalls 5

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Customed, Inc. · FAJ Cystoscope And Accessories, Flexible/Rigid

Cleared on Sep 20, 1990 after a 122-day review. FDA has not posted a summary or statement for it, so its predicates are not known. It has been recalled 5 times.

Decided
Sep 20, 1990
Review
122 days
Class
Class II
Product code
FAJ
Recalls
5
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K902274Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FAJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new FAJ device

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  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Jan 7, 2016Class IIZ-1407-2016PackagingRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Jan 7, 2016Class IIZ-1463-2016PackagingRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Jul 10, 2015Class IIZ-2678-2015PackagingRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Jul 10, 2015Class IIZ-2558-2015PackagingRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Jul 10, 2015Class IIZ-2660-2015PackagingRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

No ancestor or descendant has a Class I recall.

How does its category compare?

All FAJ devices

FAJ Cystoscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FAJ

8in 2025

2007: 22009: 22010: 12012: 12014: 12016: 12017: 22018: 22019: 32020: 22021: 32022: 52023: 52024: 92025: 82026 (partial year): 5
2007high 9 (2024) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FAJ

98in 2025

2019: 207 days median2021: 127 days median2022: 170 days median2023: 207 days median2024: 130 days median2025: 98 days median2026 (partial year): 123 days median
2007high 207 (2019) · low 98 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FAJ

7in 2023

2017: 12022: 12023: 7
2007high 7 (2023) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FAJ

2,690in 2025

2007: 92008: 102009: 102010: 92011: 132012: 82013: 122014: 62015: 282016: 752017: 792018: 792019: 1022020: 3392021: 4942022: 7442023: 9202024: 8922025: 2,690
2007high 2,690 (2025) · low 6 (2014)2025

MAUDE reports naming product code FAJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—09
20080—010
20092—010
20101—09
20110—013
20121—08
20130—012
20141—06
20150—028
20161—075
20172—179
20182—079
201932070102
20202—0339
202131270494
202251701744
202352077920
202491300892
202589802,690
202651230—
Cite this page

510(k) Report. “K902274: Customed Cysto Pack I.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K902274

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026