FDA product code · General Hospital · Class 2
QNQ: Low Dead Space Piston Syringe
QNQ is FDA's product code for "Low Dead Space Piston Syringe": a Class 2 device classified under 21 CFR 880.5860, reviewed by the General Hospital panel.
510(k) review time for QNQ
Across 12 510(k) clearances under QNQ decided from 2018-01-01 to 2026-10-06, the median was 181 days from FDA receipt to decision. Half took between 101 and 291 days, and 80% were decided within 344 days. These are past clearances, not a forecast for a new submission.
| Fastest | 0 |
|---|---|
| 25th percentile | 101 |
| Median | 181 |
| 75th percentile | 291 |
| 80th percentile | 344 |
| 90th percentile | 437 |
| Slowest | 618 |
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.
FDA-recognized standards that cite QNQ
No FDA recognized consensus standard cites QNQ 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.