510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K163472Substantially Equivalent

Intra.Ox Handheld Tissue Oximeter

Vioptix, Inc., Newark CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K163472 is the FDA 510(k) clearance record for Intra.Ox Handheld Tissue Oximeter, a class II device, cleared for Vioptix, Inc. on under FDA product code MUD (Oximeter, Tissue Saturation). FDA records list 9 510(k) clearances for Vioptix, Inc., from to . As of , FDA records show no recalls naming K163472.

Clearance record

Decision date
Received
(339 days to decision)
Product code
MUD Oximeter, Tissue Saturation
Regulation
21 CFR 870.2700
Device class
Class II
Review panel
Cardiovascular
Applicant
Vioptix, Inc. 39655 Eureka Dr., Newark CA
510(k) summary
Summary PDF
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