FDA product code · Gastroenterology, Urology · Class 2
FET: Endoscopic Video Imaging System/Component, Gastroenterology-Urology
FET is FDA's product code for "Endoscopic Video Imaging System/Component, Gastroenterology-Urology": a Class 2 device classified under 21 CFR 876.1500, reviewed by the Gastroenterology, Urology panel.
510(k) review time for FET
Across 26 510(k) clearances under FET decided from 2018-01-01 to 2026-10-06, the median was 109 days from FDA receipt to decision. Half took between 58 and 170 days, and 80% were decided within 178 days. These are past clearances, not a forecast for a new submission.
| Fastest | 16 |
|---|---|
| 25th percentile | 58 |
| Median | 109 |
| 75th percentile | 170 |
| 80th percentile | 178 |
| 90th percentile | 248 |
| Slowest | 284 |
| Year | Median days | n |
|---|---|---|
| 2020 | 106 | 5 |
| 2025 | 166 | 6 |
Source: openFDA 510(k) records, snapshot of 2026-10-06 (openFDA data as of 2026-09-28). Compare 510(k) review times across all device types, see every code side by side in the Clearance Timeline Estimator, or browse the clearances themselves in PredicateScope.
FET in the public FDA record
| 510(k) clearances, all years | 100 |
|---|---|
| Device recalls | 8 |
| Establishment listings | 281 |
Counts of records, not of devices or events. Adverse event reports for FET are in MAUDEScope, as counts with the query shown: MAUDE has no denominator, so a report count is not a rate and does not show that a device caused an event.
FDA-recognized standards that cite FET
No FDA recognized consensus standard cites FET by product code. Horizontal standards such as biocompatibility, sterilization and software standards can still apply.
Source: FDA Recognized Consensus Standards, snapshot of 2026-09-01. Search them all in the Consensus Standards Lookup.