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FDA 510(k)

NEBULIZER PUMP POWERED MODELS 020 AND 050

K-Number: K883132 · 1988-10-18

Decision Date1988-10-18
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER PUMP POWERED MODELS 020 AND 050 is the device name listed in this FDA 510(k) record. The listed applicant is Travelneb, Inc.. It received FDA 510(k) clearance on 1988-10-18 under 510(k) number K883132. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEBULIZER PUMP POWERED MODELS 020 AND 050?

NEBULIZER PUMP POWERED MODELS 020 AND 050 is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Travelneb, Inc.. The 510(k) number is K883132.

When did NEBULIZER PUMP POWERED MODELS 020 AND 050 receive FDA 510(k) clearance?

NEBULIZER PUMP POWERED MODELS 020 AND 050 received FDA 510(k) clearance on 1988-10-18, under 510(k) number K883132.

Who is the listed applicant for NEBULIZER PUMP POWERED MODELS 020 AND 050?

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

What is the FDA product code for NEBULIZER PUMP POWERED MODELS 020 AND 050?

The FDA product code for NEBULIZER PUMP POWERED MODELS 020 AND 050 is BTI.

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.

Related Devices (Code: BTI)

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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