FDA product code · Cardiovascular · Class 2
DRF: Catheter, Electrode Recording, Or Probe, Electrode Recording
DRF is FDA's product code for "Catheter, Electrode Recording, Or Probe, Electrode Recording": a Class 2 device classified under 21 CFR 870.1220, reviewed by the Cardiovascular panel.
510(k) review time for DRF
Across 29 510(k) clearances under DRF decided from 2018-01-01 to 2026-10-06, the median was 146 days from FDA receipt to decision. Half took between 77 and 231 days, and 80% were decided within 269 days. These are past clearances, not a forecast for a new submission.
| Fastest | 29 |
|---|---|
| 25th percentile | 77 |
| Median | 146 |
| 75th percentile | 231 |
| 80th percentile | 269 |
| 90th percentile | 309 |
| Slowest | 695 |
| Year | Median days | n |
|---|---|---|
| 2019 | 163 | 9 |
| 2021 | 124 | 5 |
| 2022 | 283 | 5 |
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.
DRF in the public FDA record
| 510(k) clearances, all years | 185 |
|---|---|
| Device recalls | 26 |
| Establishment listings | 457 |
| GUDID device identifiers | 1,607 |
Counts of records, not of devices or events. Adverse event reports for DRF 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 DRF
No FDA recognized consensus standard cites DRF 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.