Maxtec MaxBlend2+p— 510(k) K231895

Substantially Equivalent

Maxtec, LLC

FDA 510(k) clearance K231895 for Maxtec MaxBlend2+p, Substantially Equivalent on 2023-12-04. Applicant: Maxtec, LLC. Device class: 2.

Clearance details

Applicant: Maxtec, LLC
Product code: Code BZR
Device class: Class 2
Regulation: 21 CFR 868.5330
Advisory panel: Anesthesiology
Date received: 2023-06-28
Decision date: 2023-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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More clearances from Maxtec, LLC

K221734 — Maxtec MaxO2 ME+p2023-04-01
K182362 — MaxCap Ped and MaxCap Neo2019-05-23
K161718 — MaxBlend 2, MaxBlend Lite2016-10-27
K153659 — MaxO2ME2016-06-10
K112402 — ULTRAMAXO2 OXYGEN ANALYER2011-12-14

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