Instalief— 510(k) K172358

Substantially Equivalent

Privi Medical Pte, Ltd.

FDA 510(k) clearance K172358 for Instalief, Substantially Equivalent on 2018-01-10. Applicant: Privi Medical Pte, Ltd.. Device class: Unclassified.

Clearance details

Applicant: Privi Medical Pte, Ltd.
Product code: Code LKX
Device class: Unclassified
Advisory panel: Unknown
Date received: 2017-08-03
Decision date: 2018-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Singapore, SG

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKX

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K012746 — ICE BATON2001-11-14
K981428 — ANU ICE1998-07-07

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