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EndoRotor® Catheter 3.2mm x 1270mm

INTERSCOPE, INC · Model ER 10-03-F · UDI-DI 00865830000282

PTE Prescription
2
510(k) clearances
6
Adverse events
0
Recalls
1
Facilities

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.