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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

EXG PulseLinQ Cables (EXGPL)

FDA 510(k) source

510(k) number
K262816
Applicant
Cb Innovations, LLC
Decision date
Oct 30, 2026
Date received
Aug 7, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
DSA
Device type
Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class II
Regulation
21 CFR 870.2900
Advisory committee
Cardiovascular
Statement or summary
Summary
Third party
N
Location
Carlsbad, CA, US