510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003939Substantially Equivalent

Venture Home Fill II, Model Ioh 200

Invacare GmbH, Elyria OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003939 is the FDA 510(k) clearance record for VENTURE HOME FILL II, MODEL IOH 200, a class II device, cleared for Invacare Corp. on under FDA product code CAW (Generator, Oxygen, Portable). FDA records list 131 510(k) clearances for Invacare Corp., from to . As of , FDA records show one recall naming K003939.

Clearance record

Decision date
Received
(90 days to decision)
Product code
CAW Generator, Oxygen, Portable
Regulation
21 CFR 868.5440
Device class
Class II
Review panel
Anesthesiology
Applicant
Invacare Corp. One Invacare Way, Elyria OH
510(k) summary
Summary
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