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FDA product code NMM

Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed

CardiovascularClass 221 CFR 870.1250
Verified
US regulatory classifications
US Product Code (FDA)
NMM
View Product Code Classification
US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 870.1250
View CFR Regulation
Medical specialty
Cardiovascular
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
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)

Search keywords

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01Angioplasty02Catheter03Peripheral04Transluminal05Balloon06PTA07PTCA08Reprocessed09Vascular10Cardiovascular
About this record

Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed is a medical device type in the Cardiovascular specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.