Olympus Unsaturated Iron Binding Capacity Reagent

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K955139 ↗

FDA Product Code

JMO

Device Class

Class I

Regulation

21 CFR Part 862.1415

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

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• Olympus Fb Series Biopsy Forceps

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• Olympus Biopsy Forceps Model Fb-44

  Class II

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• Olympus Um 2R/3R Ultrasonic Probes and Associated Ancillary Equipment, for Bronchial Use

  Class II

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See all devices from Olympus America, Inc. →