510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K873156Substantially Equivalent

Amox Oxygen Generators

Vbm Corp., Louisville KY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873156 is the FDA 510(k) clearance record for AMOX OXYGEN GENERATORS, a class II device, cleared for Vbm Corp. on under FDA product code CAW (Generator, Oxygen, Portable). FDA records list one 510(k) clearance for Vbm Corp. As of , FDA records show no recalls naming K873156.

Clearance record

Decision date
Received
(175 days to decision)
Product code
CAW Generator, Oxygen, Portable
Regulation
21 CFR 868.5440
Device class
Class II
Review panel
Anesthesiology
Applicant
Vbm Corp. Post Office Box 922, Louisville KY
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