STATUSBLUE
K-Number: K013237 · 2001-10-22
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Device Summary
Frequently Asked Questions
What is the STATUSBLUE?
STATUSBLUE is a medical device that received FDA 510(k) clearance on 2001-10-22. The listed applicant is Dmg USA, Inc.. The 510(k) number is K013237.
When did STATUSBLUE receive FDA 510(k) clearance?
STATUSBLUE received FDA 510(k) clearance on 2001-10-22, under 510(k) number K013237.
Who is the listed applicant for STATUSBLUE?
The FDA 510(k) record lists Dmg USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STATUSBLUE?
The FDA product code for STATUSBLUE is ELW.
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 Dmg USA, 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: ELW)
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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