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510(k) K120277

VITAL COUGH by Lung Assist, Inc. — Product Code NHJ

K120277 is an FDA 510(k) premarket notification submitted by Lung Assist, Inc. for the device "VITAL COUGH". The FDA issued a decision of Substantially Equivalent on September 12, 2012. The device falls under product code NHJ (Device, Positive Pressure Breathing, Intermittent), a Class II device regulated under 21 CFR 868.5905. Lung Assist, Inc. has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 12, 2012
Date Received
January 30, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Positive Pressure Breathing, Intermittent
Device Class
Class II
Regulation Number
868.5905
Review Panel
AN
Submission Type

Other clearances by Lung Assist, Inc.

  • K132988 — VITAL COUGH (March 28, 2014)

Other clearances for product code NHJ

  • K253001 — KT Airway Clearance Device II (KT-3); KT Airway Clearance Device II (KT-5) (June 16, 2026)
  • K242438 — Clearo (May 16, 2025)
  • K231728 — BiWaze Clear System (April 8, 2024)
  • K213564 — BiWaze Clear System (December 21, 2022)
  • K200988 — Maximus System (May 26, 2020)
  • K191912 — BiWaze Cough (March 27, 2020)
  • K192143 — Maximus System (February 14, 2020)
  • K151689 — MetaNeb 4 System (March 17, 2016)
  • K140598 — PEGASO COUGH, PEGASO A-COUGH, PEGASO A-COUGH PERC (October 16, 2014)
  • K140605 — MINIPEGASO COUGH, MINIPEGASO A-COUGH, MINIPEGASO A-COUG PERC (October 3, 2014)

FDA data resources