MACHNET CAROTIDS COIL ARRAY ASSEMBLY
K-Number: K012491 · 2001-10-24
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Device Summary
Frequently Asked Questions
What is the MACHNET CAROTIDS COIL ARRAY ASSEMBLY?
MACHNET CAROTIDS COIL ARRAY ASSEMBLY is a medical device that received FDA 510(k) clearance on 2001-10-24. The listed applicant is Machnet BV. The 510(k) number is K012491.
When did MACHNET CAROTIDS COIL ARRAY ASSEMBLY receive FDA 510(k) clearance?
MACHNET CAROTIDS COIL ARRAY ASSEMBLY received FDA 510(k) clearance on 2001-10-24, under 510(k) number K012491.
Who is the listed applicant for MACHNET CAROTIDS COIL ARRAY ASSEMBLY?
The FDA 510(k) record lists Machnet BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MACHNET CAROTIDS COIL ARRAY ASSEMBLY?
The FDA product code for MACHNET CAROTIDS COIL ARRAY ASSEMBLY is MOS.
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 Machnet BV 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: MOS)
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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