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Model note · Nebulizer

PARI LC Sprint Reusable Nebulizer

The LC Sprint is a reusable, breath enhanced jet nebuliser for single patient use, driven by a compressor or piped air. A two way valve system opens the inspiratory valve on inhalation and vents exhaled air through the mouthpiece valve, which reduces wasted aerosol. It is used in homes, clinics and hospitals for adults and children with prescribed nebulised medicines, and has no electronics.

The model

Maker, model and type.

Maker
PARI GmbH (US: PARI Respiratory Equipment / PARI Innovative Manufacturers, Inc.)
Model
LC Sprint Reusable Nebulizer
Device type
Nebulizer
Main document
Open the public document

Key specifications

What the public record says.

ItemValueSource
Drive gas requirement3.5 to 8 L/min at a minimum of 20 psi to achieve the specified droplet characteristicsSource
Aerosol with PARI BOY compressor (ISO 27427, salbutamol)Respirable drug delivery rate 99 uL/min; MMAD 3.8 um; 62% of mass below 5 umSource
Maximum fill8 mLSource
PartsInspiratory valve cap, nebuliser top, insert, cup, mouthpiece with expiratory valve, Wing Tip tubingSource
Replacement and warrantyReplace the reusable cup every six months; 6 month limited home care warrantySource
FDA clearanceK060399, LC Sprint Reusable Nebulizer, product code CAF, Class II, 21 CFR 868.5630, March 2006; predicates Misty Max 10 and PARI LC StarSource

Recalls

Recalls.

This note lists no recalls. Check the FDA recall database for the latest record.

Safety

Safety warnings from the record.

  • Clean and dry all parts after every treatment and disinfect regularly; contamination can cause serious or fatal illness. Source
  • Single patient use only; never share a nebuliser between patients. Source
  • Small parts are a choking hazard and tubing a strangulation hazard, so supervise children closely and never use while drowsy. Source
  • Children under 4 and patients with special needs should use a mask rather than the mouthpiece. Source

Sources

Where this note comes from.

Not covered: The LC Sprint is a purely mechanical device with no error codes. openFDA has no recall records and only one MAUDE report for the brand. Aerosol figures apply to the PARI BOY compressor and differ for other drive sources.

BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.

Nebulizer

Other models of this device.