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FDA 510(k)

NEUROLOGICAL ENDOSCOPE

K-Number: K970162 · 1997-10-29

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1997-10-29
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROLOGICAL ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1997-10-29 under 510(k) number K970162. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROLOGICAL ENDOSCOPE?

NEUROLOGICAL ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1997-10-29. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K970162.

When did NEUROLOGICAL ENDOSCOPE receive FDA 510(k) clearance?

NEUROLOGICAL ENDOSCOPE received FDA 510(k) clearance on 1997-10-29, under 510(k) number K970162.

Who is the listed applicant for NEUROLOGICAL ENDOSCOPE?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROLOGICAL ENDOSCOPE?

The FDA product code for NEUROLOGICAL ENDOSCOPE is GWG.

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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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