510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K042944Substantially Equivalent

Home-Away System, Model 1041

In-X Corp., Denver CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042944 is the FDA 510(k) clearance record for HOME-AWAY SYSTEM, MODEL 1041, a class II device, cleared for In-X Corporation on under FDA product code CAW (Generator, Oxygen, Portable). FDA records list 2 510(k) clearances for In-X Corporation, from to . As of , FDA records show no recalls naming K042944.

Clearance record

Decision date
Received
(172 days to decision)
Product code
CAW Generator, Oxygen, Portable
Regulation
21 CFR 868.5440
Device class
Class II
Review panel
Anesthesiology
Applicant
In-X Corporation 6753 E. 47th Ave., Denver CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CAW

Trailing 12 months
12 clearances under product code CAW in the twelve months to October 2026, December 2025 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code CAW, trailing twelve months
MonthClearances
November 20251
December 20255
January 20260
February 20260
March 20261
April 20261
May 20261
June 20261
July 20260
August 20261
September 20261
October 20260