MEDITECH MODEL ABPM-04
K-Number: K051149 · 2005-11-18
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Device Summary
Frequently Asked Questions
What is the MEDITECH MODEL ABPM-04?
MEDITECH MODEL ABPM-04 is a medical device that received FDA 510(k) clearance on 2005-11-18. The listed applicant is Meditech Kft.. The 510(k) number is K051149.
When did MEDITECH MODEL ABPM-04 receive FDA 510(k) clearance?
MEDITECH MODEL ABPM-04 received FDA 510(k) clearance on 2005-11-18, under 510(k) number K051149.
Who is the listed applicant for MEDITECH MODEL ABPM-04?
The FDA 510(k) record lists Meditech Kft. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDITECH MODEL ABPM-04?
The FDA product code for MEDITECH MODEL ABPM-04 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 Meditech Kft. 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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