510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K881420Substantially Equivalent

Omni-Vent, Series D/mri

Stein-Gates Medical Equipment, Inc., Atchison KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881420 is the FDA 510(k) clearance record for OMNI-VENT, SERIES D/MRI, a class II device, cleared for Stein-Gates Medical Equipment, Inc. on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 2 510(k) clearances for Stein-Gates Medical Equipment, Inc., from to . As of , FDA records show no recalls naming K881420.

Clearance record

Decision date
Received
(71 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Stein-Gates Medical Equipment, Inc. 121 N. Fourth St., Atchison KS
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260