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FDA 510(k)

MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123

K-Number: K013027 · 2001-12-06

Decision Date2001-12-06
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123 is the device name listed in this FDA 510(k) record. The listed applicant is Respironics Healthscan, Inc.. It received FDA 510(k) clearance on 2001-12-06 under 510(k) number K013027. 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 MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123?

MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123 is a medical device that received FDA 510(k) clearance on 2001-12-06. The listed applicant is Respironics Healthscan, Inc.. The 510(k) number is K013027.

When did MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123 receive FDA 510(k) clearance?

MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123 received FDA 510(k) clearance on 2001-12-06, under 510(k) number K013027.

Who is the listed applicant for MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123?

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

What is the FDA product code for MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123?

The FDA product code for MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123 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.

Other records listing Respironics Healthscan, 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.

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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