510(k) K261389

PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1) by Salter Labs — Product Code CCL

K261389 is an FDA 510(k) premarket notification submitted by Salter Labs for the device "PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)". The FDA issued a decision of Substantially Equivalent on July 30, 2026. The device falls under product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase), a Class II device regulated under 21 CFR 868.1720. Salter Labs has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 30, 2026
Date Received
April 28, 2026
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Gas, Oxygen, Gaseous-Phase
Device Class
Class II
Regulation Number
868.1720
Review Panel
AN
Submission Type