OMRON COMPRESSOR NEBULIZER- MODEL NE-C09
K-Number: K914836 · 1992-05-06
Advertisement
Device Summary
Frequently Asked Questions
What is the OMRON COMPRESSOR NEBULIZER- MODEL NE-C09?
OMRON COMPRESSOR NEBULIZER- MODEL NE-C09 is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K914836.
When did OMRON COMPRESSOR NEBULIZER- MODEL NE-C09 receive FDA 510(k) clearance?
OMRON COMPRESSOR NEBULIZER- MODEL NE-C09 received FDA 510(k) clearance on 1992-05-06, under 510(k) number K914836.
Who is the listed applicant for OMRON COMPRESSOR NEBULIZER- MODEL NE-C09?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON COMPRESSOR NEBULIZER- MODEL NE-C09?
The FDA product code for OMRON COMPRESSOR NEBULIZER- MODEL NE-C09 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 Omron Healthcare, 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement