Jovus Eagle Eye F/X 2.9F Ivus Catheter, Model 85900

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K031346 ↗

FDA Product Code

OBJ

Device Class

Class II

Regulation

21 CFR Part 870.1200

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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See all devices from Jomed AG →