NEONATE ARRAY COILS
K-Number: K091047 · 2010-08-18
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Device Summary
Frequently Asked Questions
What is the NEONATE ARRAY COILS?
NEONATE ARRAY COILS is a medical device that received FDA 510(k) clearance on 2010-08-18. The listed applicant is Lmt Medical Systems GmbH. The 510(k) number is K091047.
When did NEONATE ARRAY COILS receive FDA 510(k) clearance?
NEONATE ARRAY COILS received FDA 510(k) clearance on 2010-08-18, under 510(k) number K091047.
Who is the listed applicant for NEONATE ARRAY COILS?
The FDA 510(k) record lists Lmt Medical Systems GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEONATE ARRAY COILS?
The FDA product code for NEONATE ARRAY COILS 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 Lmt Medical Systems GmbH 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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