FDA product code · Neurology · Class 2
MOF: Guide, Wire, Catheter, Neurovasculature
MOF is FDA's product code for "Guide, Wire, Catheter, Neurovasculature": a Class 2 device classified under 21 CFR 870.1330, reviewed by the Neurology panel.
510(k) review time for MOF
Across 33 510(k) clearances under MOF decided from 2018-01-01 to 2026-10-06, the median was 163 days from FDA receipt to decision. Half took between 30 and 226 days, and 80% were decided within 232 days. These are past clearances, not a forecast for a new submission.
| Fastest | 24 |
|---|---|
| 25th percentile | 30 |
| Median | 163 |
| 75th percentile | 226 |
| 80th percentile | 232 |
| 90th percentile | 262 |
| Slowest | 392 |
| Year | Median days | n |
|---|---|---|
| 2025 | 172 | 5 |
| 2026 (to 10-06, partial) | 192 | 11 |
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.
MOF in the public FDA record
| 510(k) clearances, all years | 44 |
|---|---|
| Establishment listings | 96 |
Counts of records, not of devices or events. Adverse event reports for MOF 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 MOF
No FDA recognized consensus standard cites MOF 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.