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FDA 510(k)

EZFLOW CONTINUOUS NEBULIZER,MODEL 1005

K-Number: K990384 · 1999-04-26

Decision Date1999-04-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EZFLOW CONTINUOUS NEBULIZER,MODEL 1005 is the device name listed in this FDA 510(k) record. The listed applicant is Piper Medical Products. It received FDA 510(k) clearance on 1999-04-26 under 510(k) number K990384. 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 EZFLOW CONTINUOUS NEBULIZER,MODEL 1005?

EZFLOW CONTINUOUS NEBULIZER,MODEL 1005 is a medical device that received FDA 510(k) clearance on 1999-04-26. The listed applicant is Piper Medical Products. The 510(k) number is K990384.

When did EZFLOW CONTINUOUS NEBULIZER,MODEL 1005 receive FDA 510(k) clearance?

EZFLOW CONTINUOUS NEBULIZER,MODEL 1005 received FDA 510(k) clearance on 1999-04-26, under 510(k) number K990384.

Who is the listed applicant for EZFLOW CONTINUOUS NEBULIZER,MODEL 1005?

The FDA 510(k) record lists Piper Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZFLOW CONTINUOUS NEBULIZER,MODEL 1005?

The FDA product code for EZFLOW CONTINUOUS NEBULIZER,MODEL 1005 is CAF.

Related Clinical Trials

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.

Other records listing Piper Medical Products 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.

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.

Official Source

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

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