510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K120277Substantially Equivalent

Vital Cough

Lung Assist, Inc., Boulder CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120277 is the FDA 510(k) clearance record for VITAL COUGH, a class II device, cleared for Lung Assist, Inc. on under FDA product code NHJ (Device, Positive Pressure Breathing, Intermittent). FDA records list 2 510(k) clearances for Lung Assist, Inc., from to . As of , FDA records show no recalls naming K120277.

Clearance record

Decision date
Received
(226 days to decision)
Product code
NHJ Device, Positive Pressure Breathing, Intermittent
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Lung Assist, Inc. 4655 Kirkwood Ct., Boulder CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NHJ

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