NEUROVISION MEDICAL MOTION SENSOR
K-Number: K130570 · 2013-12-26
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Device Summary
Frequently Asked Questions
What is the NEUROVISION MEDICAL MOTION SENSOR?
NEUROVISION MEDICAL MOTION SENSOR is a medical device that received FDA 510(k) clearance on 2013-12-26. The listed applicant is Neurovision Medical Products, Inc.. The 510(k) number is K130570.
When did NEUROVISION MEDICAL MOTION SENSOR receive FDA 510(k) clearance?
NEUROVISION MEDICAL MOTION SENSOR received FDA 510(k) clearance on 2013-12-26, under 510(k) number K130570.
Who is the listed applicant for NEUROVISION MEDICAL MOTION SENSOR?
The FDA 510(k) record lists Neurovision Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROVISION MEDICAL MOTION SENSOR?
The FDA product code for NEUROVISION MEDICAL MOTION SENSOR is BZQ.
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 Neurovision Medical Products, Inc. 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: BZQ)
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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