MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123
K-Number: K013027 · 2001-12-06
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Device Summary
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
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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