STOCKERT NEURO N50, MODEL12267
K-Number: K070336 · 2007-06-14
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Device Summary
Frequently Asked Questions
What is the STOCKERT NEURO N50, MODEL12267?
STOCKERT NEURO N50, MODEL12267 is a medical device that received FDA 510(k) clearance on 2007-06-14. The listed applicant is Stockert GmbH. The 510(k) number is K070336.
When did STOCKERT NEURO N50, MODEL12267 receive FDA 510(k) clearance?
STOCKERT NEURO N50, MODEL12267 received FDA 510(k) clearance on 2007-06-14, under 510(k) number K070336.
Who is the listed applicant for STOCKERT NEURO N50, MODEL12267?
The FDA 510(k) record lists Stockert GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOCKERT NEURO N50, MODEL12267?
The FDA product code for STOCKERT NEURO N50, MODEL12267 is GXD.
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 Stockert 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: GXD)
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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