510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K241393Substantially Equivalent

ODI-Tech

Odi Medical AS, Oslo, NO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K241393 is the FDA 510(k) clearance record for ODI-Tech, a class II device, cleared for Odi Medical AS on under FDA product code MUD (Oximeter, Tissue Saturation). FDA records list one 510(k) clearance for Odi Medical AS. As of , FDA records show no recalls naming K241393.

Clearance record

Decision date
Received
(106 days to decision)
Product code
MUD Oximeter, Tissue Saturation
Regulation
21 CFR 870.2700
Device class
Class II
Review panel
Cardiovascular
Applicant
Odi Medical AS Karenslyst Allé 8a, Oslo, NO
510(k) summary
Statement
Third party review
No

Clearances, product code MUD

Trailing 12 months
1 clearance under product code MUD in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MUD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260