1.2MM REUSABLE NEUROVIEW ENDOSCOPE
K-Number: K961173 · 1996-06-07
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Device Summary
Frequently Asked Questions
What is the 1.2MM REUSABLE NEUROVIEW ENDOSCOPE?
1.2MM REUSABLE NEUROVIEW ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1996-06-07. The listed applicant is Neuro Navigational Corp.. The 510(k) number is K961173.
When did 1.2MM REUSABLE NEUROVIEW ENDOSCOPE receive FDA 510(k) clearance?
1.2MM REUSABLE NEUROVIEW ENDOSCOPE received FDA 510(k) clearance on 1996-06-07, under 510(k) number K961173.
Who is the listed applicant for 1.2MM REUSABLE NEUROVIEW ENDOSCOPE?
The FDA 510(k) record lists Neuro Navigational Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.2MM REUSABLE NEUROVIEW ENDOSCOPE?
The FDA product code for 1.2MM REUSABLE NEUROVIEW ENDOSCOPE is GWG.
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 Neuro Navigational Corp. 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: GWG)
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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