FDA product code · General, Plastic Surgery · Class 2
QRL: Multiple Use Blood Lancet For Single Patient Use Only
QRL is FDA's product code for "Multiple Use Blood Lancet For Single Patient Use Only": a Class 2 device classified under 21 CFR 878.4850, reviewed by the General, Plastic Surgery panel.
510(k) review time for QRL
Across 27 510(k) clearances under QRL decided from 2018-01-01 to 2026-10-06, the median was 88 days from FDA receipt to decision. Half took between 58 and 147 days, and 80% were decided within 165 days. These are past clearances, not a forecast for a new submission.
| Fastest | 15 |
|---|---|
| 25th percentile | 58 |
| Median | 88 |
| 75th percentile | 147 |
| 80th percentile | 165 |
| 90th percentile | 180 |
| Slowest | 249 |
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.
QRL in the public FDA record
| Establishment listings | 116 |
|---|
Counts of records, not of devices or events. Adverse event reports for QRL 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 QRL
No FDA recognized consensus standard cites QRL 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.
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