K131910 is the FDA 510(k) clearance record for MPP, a class II device, cleared for Marc Pro on 2014-01-24 under FDA product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter). FDA's definition for product code NUH reads: "TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES". FDA records list one 510(k) clearance for Marc Pro. As of 2026-09-10 , FDA records show no recalls naming K131910.
Clearance record Decision date 2014-01-24 Received 2013-06-26 (212 days to decision) Product code NUH Stimulator, Nerve, Transcutaneous, Over-The-CounterRegulation 21 CFR 882.5890 Device class Class II Review panel Neurology Applicant Marc Pro 3722 Ave. Sausalito, Irvine CA 510(k) summary Summary PDF ↗ Third party review No
Clearances, product code NUH Trailing 12 months 10 clearances under product code NUH in the twelve months to October 2026, November 2025 the highest month at 3. Show the numbers FIRST ARTICLE / WEEKLY
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Product code NUH
FDA records show no recalls under product code NUH.
MDM coverage of this record lists here, newest first.
About this record Sourced from the FDA 510(k) premarket notification database, ingested from openFDA. MDM adds the decision time in days, the product code cross-link, recalls sharing that product code, and MDM coverage of the record.
Predicate devices are not listed. The openFDA 510(k) endpoint does not publish predicate references, so MDM does not assert them. Where a 510(k) summary exists, the FDA PDF is linked above and names the predicate itself.
Data as of 2026-09-28 , the FDA export date for this dataset. Page last changed 2026-09-05 . View this record on fda.gov ↗ (opens on fda.gov)
