AUTOMOVE, MODEL AM800
K-Number: K032955 · 2003-12-15
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Device Summary
Frequently Asked Questions
What is the AUTOMOVE, MODEL AM800?
AUTOMOVE, MODEL AM800 is a medical device that received FDA 510(k) clearance on 2003-12-15. The listed applicant is Danmeter A/S. The 510(k) number is K032955.
When did AUTOMOVE, MODEL AM800 receive FDA 510(k) clearance?
AUTOMOVE, MODEL AM800 received FDA 510(k) clearance on 2003-12-15, under 510(k) number K032955.
Who is the listed applicant for AUTOMOVE, MODEL AM800?
The FDA 510(k) record lists Danmeter A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOMOVE, MODEL AM800?
The FDA product code for AUTOMOVE, MODEL AM800 is IPF.
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 Danmeter A/S 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: IPF)
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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