FDA Device Establishments · JSON-LD · Markdown

KONICA MINOLTA, INC.

FEI 3003769120 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3003769120
Owner / OperatorKONICA MINOLTA, INC. (#9009884)
Address2970 ISHIKAWA-MACHI, HACHIOJI-SHI Tokyo, 192-8505, JP
Mandatory US AgentKonica Minolta Healthcare Americas, Inc.
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)MQB, LLZ
Regulation § (21 CFR)892.1680, 892.2050
Proprietary namesG-60; G-22; P-75; CS-7; P-65; SKR 3000; G-59

External sources

Source: openFDA. Public-domain (CC0).