510(k) K231895

Device
Maxtec MaxBlend2+p
Applicant
Maxtec, LLC
510(k) number
K231895
Product code
BZR
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-04
Date received
2023-06-28
Regulation
868.5330
Classification name
Mixer, Breathing Gases, Anesthesia Inhalation
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Sidra Hankins
Address
2305 S 1070 W Salt Lake City UT US 84119 84119

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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