Modification to: Eflow Electronic Inhaler/Nebulizer

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K072670 ↗

FDA Product Code

CAF

Device Class

Class II

Regulation

21 CFR Part 868.5630

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Pari Hydrate V

  Class II

  FDA 510(k) K072982 Active Cleared 29 Nov 2007

• Eflow Electronic Inhaler/Nebulizer

  Class II

  FDA 510(k) K033833 Active Cleared 5 May 2004

• Trek S Nebulizer Compressor

  Class II

  FDA 510(k) K060357 Active Cleared 5 Apr 2006

• Lc Sprint Nebulizer

  Class II

  FDA 510(k) K060399 Active Cleared 2 Mar 2006

• Lc Sprint Star

  Class II

  FDA 510(k) K062158 Active Cleared 28 Aug 2006

• Lc Star with Nasal Adapter

  Class II

  FDA 510(k) K061381 Active Cleared 2 Jun 2006

See all devices from Pari Innovative Manufacturers, Inc. →