NMM

Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed

Product code: NMM
Device name: Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed
Device class: Class 2
21 CFR: 21 CFR 870.1250
Medical specialty: Cardiovascular
Marketing pathway: 510(K)

FDA classification definition

Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf)

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: NMM

Classification and pathway per current FDA publications. Data from openFDA (CC0).