FDA product code · Cardiovascular · Class 2

PPN: Percutaneous Catheter, Ultrasound

PPN is FDA's product code for "Percutaneous Catheter, Ultrasound": a Class 2 device classified under 21 CFR 870.1250, reviewed by the Cardiovascular panel.

510(k) review time for PPN

Across 12 510(k) clearances under PPN decided from 2018-01-01 to 2026-10-06, the median was 57 days from FDA receipt to decision. Half took between 29 and 111 days, and 80% were decided within 123 days. These are past clearances, not a forecast for a new submission.

Days from FDA receipt to 510(k) decision, PPN, decisions 2018-01-01 to 2026-10-06 (n = 12)
Fastest17
25th percentile29
Median57
75th percentile111
80th percentile123
90th percentile154
Slowest209

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 PPN

No FDA recognized consensus standard cites PPN 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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