HONEYWELL HOMMED CENTRAL STATION 4.0
K-Number: K072272 · 2007-09-07
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Device Summary
Frequently Asked Questions
What is the HONEYWELL HOMMED CENTRAL STATION 4.0?
HONEYWELL HOMMED CENTRAL STATION 4.0 is a medical device that received FDA 510(k) clearance on 2007-09-07. The listed applicant is Honeywell Hommed, LLC. The 510(k) number is K072272.
When did HONEYWELL HOMMED CENTRAL STATION 4.0 receive FDA 510(k) clearance?
HONEYWELL HOMMED CENTRAL STATION 4.0 received FDA 510(k) clearance on 2007-09-07, under 510(k) number K072272.
Who is the listed applicant for HONEYWELL HOMMED CENTRAL STATION 4.0?
The FDA 510(k) record lists Honeywell Hommed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HONEYWELL HOMMED CENTRAL STATION 4.0?
The FDA product code for HONEYWELL HOMMED CENTRAL STATION 4.0 is DXN.
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 Honeywell Hommed, LLC 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: DXN)
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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