RP Check (RP01)— 510(k) K260671

Substantially Equivalent

MD Diagnostics, Ltd.

FDA 510(k) clearance K260671 for RP Check (RP01), Substantially Equivalent on 2026-10-26. Applicant: MD Diagnostics, Ltd.. Device class: 2.

Clearance details

Applicant: MD Diagnostics, Ltd.
Product code: Product code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 2026-03-02
Decision date: 2026-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatham, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.