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FDA 510(k)

LC SPRINT NEBULIZER

K-Number: K060399 · 2006-03-02

ApplicantPari Innovative Manufacturers, Inc.
Decision Date2006-03-02
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LC SPRINT NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Pari Innovative Manufacturers, Inc.. It received FDA 510(k) clearance on 2006-03-02 under 510(k) number K060399. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LC SPRINT NEBULIZER?

LC SPRINT NEBULIZER is a medical device that received FDA 510(k) clearance on 2006-03-02. The listed applicant is Pari Innovative Manufacturers, Inc.. The 510(k) number is K060399.

When did LC SPRINT NEBULIZER receive FDA 510(k) clearance?

LC SPRINT NEBULIZER received FDA 510(k) clearance on 2006-03-02, under 510(k) number K060399.

Who is the listed applicant for LC SPRINT NEBULIZER?

The FDA 510(k) record lists Pari Innovative Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LC SPRINT NEBULIZER?

The FDA product code for LC SPRINT NEBULIZER is CAF.

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Other records listing Pari Innovative Manufacturers, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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